Label: GEMCITABINE injection, powder, lyophilized, for solution
GEMCITABINE- gemcitabine injection, powder, lyophilized, for solution

  • NDC Code(s): 63323-102-94, 63323-125-94
  • Packager: Fresenius Kabi USA, LLC
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated September 12, 2019

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  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use GEMCITABINE FOR INJECTION, USP safely and effectively. See full prescribing information for GEMCITABINE FOR INJECTION, USP.



    GEMCITABINE for injection, USP, for intravenous use



    Initial U.S. Approval:1996

    INDICATIONS AND USAGE

    Gemcitabine for Injection is a nucleoside metabolic inhibitor indicated:
    • in combination with carboplatin, for the treatment of advanced ovarian cancer that has relapsed at least 6 months after completion of platinum-based therapy. ( 1.1)
    • in combination with paclitaxel, for first-line treatment of metastatic breast cancer after failure of prior anthracycline-containing adjuvant chemotherapy, unless anthracyclines were clinically contraindicated. ( 1.2)
    • in combination with cisplatin, for the treatment of non-small cell lung cancer. ( 1.3)
    • as a single agent for the treatment of pancreatic cancer. ( 1.4)

    DOSAGE AND ADMINISTRATION

    Gemcitabine for Injection is for intravenous use only.
    • Ovarian Cancer: 1,000 mg/m 2 over 30 minutes on Days 1 and 8 of each 21-day cycle. ( 2.1)
    • Breast Cancer: 1,250 mg/m 2 over 30 minutes on Days 1 and 8 of each 21-day cycle.  (2.2)
    • Non-Small Cell Lung Cancer: 1,000 mg/m over 30 minutes on Days 1, 8, and 15 of each 28-day cycle or 1,250 mg/m 2  over 30 minutes on Days 1 and 8 of each 21-day cycle.  (2.3)
    • Pancreatic Cancer: 1,000 mg/m 2 over 30 minutes once weekly for the first 7 weeks, then one week rest, then once weekly for 3 weeks of each 28-day cycle.  (2.4)

    DOSAGE FORMS AND STRENGTHS

    For injection: 200 mg or 1 g lyophilized powder or cake in single-dose vials for reconstitution. ( 3)

    CONTRAINDICATIONS

    Patients with a known hypersensitivity to gemcitabine. (4)

    WARNINGS AND PRECAUTIONS

    • Schedule-Dependent Toxicity: Increased toxicity with infusion time greater than 60 minutes or dosing more frequently than once weekly. ( 5.1)
    • Myelosuppression: Monitor for myelosuppression prior to each cycle and reduce or withhold dose for severe myelosuppression. ( 5.2, 5.7
    • Pulmonary Toxicity and Respiratory Failure: discontinue gemcitabine for unexplained dyspnea or other evidence of severe pulmonary toxicity.  (5.3)
    • Hemolytic-Uremic Syndrome (HUS): Monitor renal function prior to initiation and during treatment. Discontinue gemcitabine for HUS or severe renal impairment. (5.4)
    • Hepatic Toxicity: Monitor hepatic function prior to initiation and during treatment. Discontinue gemcitabine for severe hepatic toxicity.  (5.5)
    • Embryo-Fetal Toxicity: Can cause fetal harm. Advise females and males of reproductive potential to use effective contraception. ( 5.6, 8.1)
    • Exacerbation of Radiation Therapy Toxicity: May cause severe and life-threatening toxicity when administered during or within 7 days of radiation therapy. ( 5.7
    • Capillary Leak Syndrome: Discontinue gemcitabine.  (5.8)
    • Posterior Reversible Encephalopathy Syndrome (PRES): Discontinue gemcitabine.  (5.9)

    ADVERSE REACTIONS

    The most common adverse reactions for the single agent (≥20%) are nausea/vomiting, anemia, increased aspartate aminotransferase (AST), increased alanine aminotransferase (ALT), neutropenia, increased alkaline phosphatase, proteinuria, fever, hematuria, rash, thrombocytopenia, dyspnea, and edema. ( 6.1)

    To report SUSPECTED ADVERSE REACTIONS, contact Fresenius Kabi USA, LLC at 1-800-551-7176 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    USE IN SPECIFIC POPULATIONS

    Lactation: Advise not to breastfeed. ( 8.2)

    See 17 for PATIENT COUNSELING INFORMATION.

    Revised: 6/2019

  • Table of Contents
  • 1 INDICATIONS AND USAGE

    1.1 Ovarian Cancer

    Gemcitabine for Injection in combination with carboplatin is indicated for the treatment of patients with advanced ovarian cancer that has relapsed at least 6 months after completion of platinum-based therapy.

    1.2 Breast Cancer

    Gemcitabine for Injection in combination with paclitaxel is indicated for the first-line treatment of patients with metastatic breast cancer after failure of prior anthracycline-containing adjuvant chemotherapy, unless anthracyclines were clinically contraindicated.

    1.3 Non-Small Cell Lung Cancer

    Gemcitabine for Injection in combination with cisplatin is indicated for the first-line treatment of patients with inoperable, locally advanced (Stage IIIA or IIIB) or metastatic (Stage IV) non-small cell lung cancer.

    1.4 Pancreatic Cancer

    Gemcitabine for Injection is indicated as first-line treatment for patients with locally advanced (nonresectable Stage II or Stage III) or metastatic (Stage IV) adenocarcinoma of the pancreas. Gemcitabine for Injection  is indicated for patients previously treated with fluorouracil.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Ovarian Cancer

    Recommended Dose and Schedule
    The recommended dosage of Gemcitabine for Injection is 1,000 mg/m 2 intravenously over 30 minutes on Days 1 and 8 of each 21-day cycle in combination with carboplatin AUC 4 administered intravenously on Day 1 after Gemcitabine for Injection administration. Refer to carboplatin prescribing information for additional information.

    Dosage Modifications
    Recommended Gemcitabine for Injection dosage modifications for myelosuppression are described in Tables 1 and 2 [see Warnings and Precautions ( 5.2)] . Refer to the recommended dosage modifications for non-hematologic adverse reactions [see Dosage and Administration ( 2.5)].


    Table 1: Recommended Dosage Modifications for Gemcitabine for Injection for Myelosuppression on Day of Treatment in Ovarian Cancer




    Treatment
    Day
    Absolute Neutrophil Count (x 106/L)Platelet
    Count
    (X 106/L)
    Dosage
    Modification
    Day 1Greater than or equal to 1,500 and Greater than or equal to 100,000 None
    Less than 1,500 or Less than 100,000 Delay Treatment Cycle
    Day 8Greater than or equal to 1,500 and Greater than or equal to 100,000 None
    1,000 to 1,499 or 75,000 to 99,999 50% of full dose
    Less than 1,000 or Less than 75,000 Hold

    Table 2: Recommended Dosage Modifications for Gemcitabine for Injection for Myelosuppression in Previous Cycle in Ovarian Cancer




    OccurrenceMyelosuppression During Treatment CycleDosage Modification
    Initial Occurrence
    • Absolute neutrophil count less than 500 x 10 6/L for more than 5 days or
    • Absolute neutrophil count less than 100 x 10 6/L for more than 3 days or
    • Febrile neutropenia or
    • Platelets less than 25,000x10 6/L or
    • Cycle delay for more than one week due to toxicity
    Permanently reduce Gemcitabine for Injection to 800 mg/m 2 on Days 1 and 8
    Subsequent OccurrenceIf any of the above toxicities occur after the initial dose reduction: Permanently reduce Gemcitabine for Injection to 800 mg/m 2 on Day 1 only

    2.2 Breast Cancer

    Recommended Dose and Schedule
    The recommended dosage of Gemcitabine for Injection is 1,250 mg/m 2 intravenously over 30 minutes on Days 1 and 8 of each 21-day cycle in combination with paclitaxel 175 mg/m 2 administered as a 3-hour intravenous infusion on Day 1 before Gemcitabine for Injection administration. Refer to paclitaxel prescribing information for additional information.

    Dosage Modifications
    Recommended Gemcitabine for Injection dosage modifications for myelosuppression are described in Table 3 [see Warnings and Precautions ( 5.2)]. Refer to the recommended dosage modifications for non-hematologic adverse reactions [see Dosage and Administration ( 2.5)].

    Table 3: Recommended Dosage Modifications for Gemcitabine for Injection for Myelosuppression on Day of Treatment in Breast Cancer

    Treatment
    Day
    Absolute Neutrophil Count (x 106/L)Platelet
    Count
    (x 106/L)
    Dosage
    Modification
    Day 1Greater than or equal to 1,500 and Greater than or equal to 100,000 None
    Less than 1,500 or Less than 100,000 Hold
    Day 8Greater than or equal to 1,200 and Greater
    than
    75,000
    None
    1,000 to 1,199 or 50,000 to 75,000 75% of full dose
    700 to 999 and Greater than or equal to 50,000 50% of full dose
    Less than 700 or Less than 50,000 Hold


    2.3 Non-Small Cell Lung Cancer

    Recommended Dose and Schedule
    28-day schedule
    The recommended dosage of Gemcitabine for Injection is 1,000 mg/m 2 intravenously over 30 minutes on Days 1, 8, and 15 of each 28-day cycle in combination with cisplatin 100 mg/m 2 administered intravenously on Day 1 after Gemcitabine for Injection administration.

    21-day schedule
    The recommended dosage of Gemcitabine for Injection is 1,250 mg/m 2 intravenously over 30 minutes on Days 1 and 8 of each 21-day cycle in combination with cisplatin 100 mg/m 2 administered intravenously on Day 1 after Gemcitabine for Injection administration.

    Refer to cisplatin prescribing information for additional information.

    Dosage Modifications
    Recommended dosage modifications for Gemcitabine for Injection myelosuppression are described in Table 4 [see Warnings and Precautions ( 5.2)]. Refer to the recommended dosage modifications for non-hematologic adverse reactions [see Dosage and Administration ( 2.5)].

    2.4 Pancreatic Cancer

    Recommended Dose and Schedule
    The recommended dosage of Gemcitabine for Injection is 1,000 mg/m 2 intravenously over 30 minutes. The recommended treatment schedule is as follows:
    • Weeks 1 to 8: weekly dosing for the first 7 weeks followed by one week rest.
    • After week 8: weekly dosing on Days 1, 8, and 15 of each 28-day cycle.

    Dosage Modifications
    Recommended dosage modifications for Gemcitabine for Injection for myelosuppression are described in Table 4 [see Warnings and Precautions ( 5.2)] . Refer to the recommended dosage modifications for non-hematologic adverse reactions [see Dosage and Administration ( 2.5)] .


    Table 4: Recommended Dosage Modifications for Gemcitabine for Injection for Myelosuppression in Pancreatic Cancer and Non-Small Cell Lung Cancer

    Absolute Neutrophil
    Count (x 106/L)
    Platelet Count (x 106/L)Dosage Modification
    Greater than or equal to 1,000 and Greater than or equal to 100,000 None
    500 to 999 or 50,000 to 99,999 75% of full dose
    Less than 500 or Less than 50,000 Hold

    2.5 Dosage Modifications for Non-Hematologic Adverse Reactions

    Permanently discontinue Gemcitabine for Injection for any of the following:
    • Unexplained dyspnea or evidence of severe pulmonary toxicity [see Warnings and Precautions ( 5.3)]
    • Hemolytic-uremic syndrome (HUS) or severe renal impairment [see Warnings and Precautions ( 5.4)]
    • Severe hepatic toxicity [see Warnings and Precautions ( 5.5)]
    • Capillary leak syndrome (CLS) [see Warnings and Precautions ( 5.8)]
    • Posterior reversible encephalopathy syndrome (PRES) [see Warnings and Precautions ( 5.9)]

    Withhold Gemcitabine for Injection or reduce dose by 50% for other Grade 3 or 4 non-hematological adverse reactions until resolved. No dose modifications are recommended for alopecia, nausea, or vomiting.

    2.6 Preparation

    • Gemcitabine for Injection vials contain no antimicrobial preservatives and are intended for single use only.
    • Gemcitabine for Injection is a cytotoxic drug. Follow applicable special handling and disposal procedures. 1
    • Exercise caution and wear gloves when preparing Gemcitabine for Injection solutions. Immediately wash the skin thoroughly or rinse the mucosa with copious amounts of water if Gemcitabine for Injection contacts the skin or mucus membranes. Death has occurred in animal studies due to dermal absorption.
    • Reconstitute the 200 mg vial with 5 mL and 1 g vial with 25 mL of 0.9% Sodium Chloride Injection, USP  to yield a gemcitabine concentration of 38 mg/mL. Reconstituted Gemcitabine for Injection is a clear, colorless to light straw-colored solution.
    • Visually inspect reconstituted product for particulate matter and discoloration. Discard if particulate matter or discoloration is observed.
    • Withdraw the calculated dose from the vial and discard any unused portion.
    • Prior to administration, dilute the reconstituted solution with 0.9% Sodium Chloride Injection, USP to a minimum final concentration of at least 0.1 mg/mL.
    • Store Gemcitabine for Injection solutions (reconstituted and diluted) at controlled room temperature of 20°C to 25°C (68°F to 77°F). Do not refrigerate as crystallization can occur. Discard Gemcitabine for Injection solutions if not used within 24 hours after reconstitution.
    • No incompatibilities have been observed with infusion bottles or polyvinyl chloride bags and administration sets.


  • 3 DOSAGE FORMS AND STRENGTHS

    For injection: 200 mg or 1 g as sterile white to off-white lyophilized powder or cake in single-dose vials for reconstitution.

  • 4 CONTRAINDICATIONS

    Gemcitabine for Injection is contraindicated in patients with a known hypersensitivity to gemcitabine. Reactions include anaphylaxis [see Adverse Reactions ( 6.1)].

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Schedule-Dependent Toxicity

    In clinical trials evaluating the maximum tolerated dose of gemcitabine, prolongation of the infusion time beyond 60 minutes or more frequent than weekly dosing resulted in an increased incidence of clinically significant hypotension, severe flu-like symptoms, myelosuppression, and asthenia. The half-life of gemcitabine is influenced by the length of the infusion [see Clinical Pharmacology ( 12.3)] . Refer to the recommended gemcitabine dosage [see Dosage and Administration ( 2.1, 2.2,2.3,  2.4)].

    5.2 Myelosuppression

    Myelosuppression manifested by neutropenia, thrombocytopenia, and anemia occurs with gemcitabine as a single agent and the risks are increased when gemcitabine is combined with other cytotoxic drugs. In clinical trials, Grade 3-4 neutropenia, anemia, and thrombocytopenia occurred in 25%, 8%, and 5%, respectively of the 979 patients who received single agent gemcitabine. The frequencies of Grade 3-4 neutropenia, anemia, and thrombocytopenia varied from 48% to 71%, 8% to 28%, and 5% to 55%, respectively, in patients receiving gemcitabine in combination with another drug [see Adverse Reactions ( 6.1)].

    Prior to each dose of gemcitabine, obtain a complete blood count (CBC) with a differential and a platelet count. Modify the dosage as recommended [see Dosage and Administration ( 2.1, 2.2, 2.3, 2.4)].

    5.3 Pulmonary Toxicity and Respiratory Failure

    Pulmonary toxicity, including interstitial pneumonitis, pulmonary fibrosis, pulmonary edema, and adult respiratory distress syndrome (ARDS), has been reported. In some cases, these pulmonary events can lead to fatal respiratory failure despite the discontinuation of therapy. The onset of pulmonary symptoms may occur up to 2 weeks after the last dose of gemcitabine [see Adverse Reactions ( 6.1, 6.2)] . Permanently discontinue gemcitabine in patients who develop unexplained dyspnea, with or without bronchospasm, or evidence of severe pulmonary toxicity.

    5.4 Hemolytic Uremic Syndrome

    Hemolytic uremic syndrome (HUS), including fatalities from renal failure or the requirement for dialysis, can occur with gemcitabine. In clinical trials, HUS occurred in 0.25% of 2429 patients. Most fatal cases of renal failure were due to HUS [see Adverse Reactions ( 6.1)].

    Assess renal function prior to initiation of gemcitabine and periodically during treatment. Consider the diagnosis of HUS in patients who develop anemia with evidence of microangiopathic hemolysis; increased bilirubin or LDH; reticulocytosis; severe thrombocytopenia; or renal failure (increased serum creatinine or BUN). Permanently discontinue gemcitabine in patients with HUS or severe renal impairment. Renal failure may not be reversible even with the discontinuation of therapy.

    5.5 Hepatic Toxicity

    Drug-induced liver injury, including liver failure and death, has been reported in patients receiving gemcitabine alone or with other potentially hepatotoxic drugs [ see Adverse Reactions ( 6.1, 6.2)] . Administration of gemcitabine in patients with concurrent liver metastases or a pre-existing medical history or hepatitis, alcoholism, or liver cirrhosis can lead to exacerbation of the underlying hepatic insufficiency. Assess hepatic function prior to initiation of gemcitabine and periodically during treatment. Permanently discontinue gemcitabine in patients who develop severe hepatic toxicity.

    5.6 Embryo-Fetal Toxicity

    Based on animal data and its mechanism of action, gemcitabine can cause fetal harm when administered to a pregnant woman. Gemcitabine was teratogenic, embryotoxic, and fetotoxic in mice and rabbits. Advise women of the potential risk to a fetus. Advise females of reproductive potential to use effective contraception during treatment with gemcitabine and for 6 months after the final dose. Advise male patients with female partners of reproductive potential to use effective contraception during treatment with gemcitabine and for 3 months following the final dose [see Use in Specific Populations ( 8.1, 8.3)].

    5.7 Exacerbation of Radiation Therapy Toxicity

    Gemcitabine is not recommended for use in combination with radiation therapy.

    Concurrent (given together or ≤7 days apart)
    Life-threatening mucositis, especially esophagitis and pneumonitis occurred in a trial in which gemcitabine was administered at a dose of 1,000 mg/m 2 to patients with non-small cell lung cancer for up to 6 consecutive weeks concurrently with thoracic radiation.

    Non-concurrent (given >7 days apart)
    Excessive toxicity has not been observed when gemcitabine is administered more than 7 days before or after radiation. Radiation recall has been reported in patients who receive gemcitabine after prior radiation.

    5.8 Capillary Leak Syndrome

    Capillary leak syndrome (CLS) with severe consequences has been reported in patients receiving gemcitabine as a single agent or in combination with other chemotherapeutic agents [see Adverse Reactions ( 6.2)] . Permanently discontinue gemcitabine if CLS develops during therapy.

    5.9 Posterior Reversible Encephalopathy Syndrome

    Posterior reversible encephalopathy syndrome (PRES) has been reported in patients receiving gemcitabine as a single agent or in combination with other chemotherapeutic agents [see Adverse Reactions ( 6.2)] . PRES can present with headache, seizure, lethargy, hypertension, confusion, blindness, and other visual and neurologic disturbances. Confirm the diagnosis of PRES with magnetic resonance imaging (MRI). Permanently discontinue gemcitabine if PRES develops during therapy.

  • 6 ADVERSE REACTIONS

    The following serious adverse reactions are discussed in greater detail in another section of the label
    • Hypersensitivity [see Contraindications ( 4)]
    • Schedule-Dependent Toxicity [ see Warnings and Precautions (5.1)]
    • Myelosuppression [see Warnings and Precautions (5.2)]
    • Pulmonary Toxicity and Respiratory Failure [ see Warnings and Precautions (5.3)]
    • Hemolytic Uremic Syndrome [ see Warnings and Precautions (5.4)]
    • Hepatic Toxicity [ see Warnings and Precautions (5.5)]
    • Exacerbation of Radiation Toxicity [ see Warnings and Precautions (5.7)]
    • Capillary Leak Syndrome [ see Warnings and Precautions (5.8)]
    • Posterior Reversible Encephalopathy Syndrome [ see Warnings and Precautions (5.9)]

    6.1 Clinical Trials Experience

    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

    Single Agent
    The data described below reflect exposure to gemcitabine as a single agent administered at doses between 800 mg/m 2 to 1,250 mg/m 2 intravenously over 30 minutes once weekly in 979 patients with various malignancies. The most common (≥20%) adverse reactions of single agent gemcitabine are nausea/vomiting, anemia, increased alanine aminotransferase (ALT), increased aspartate aminotransferase (AST), neutropenia, increased alkaline phosphatase, proteinuria, fever, hematuria, rash, thrombocytopenia, dyspnea, and edema. The most common (≥5%) Grade 3 or 4 adverse reactions were neutropenia, nausea/vomiting, increased ALT, increased alkaline phosphatase, anemia, increased AST, and thrombocytopenia. Approximately 10% of the 979 patients discontinued gemcitabine due to adverse reactions. Adverse reactions resulting in discontinuation of gemcitabine in 2% of 979 patients were cardiovascular adverse events (myocardial infarction, cerebrovascular accident, arrhythmia, and hypertension) and adverse reactions resulting in discontinuation of gemcitabine in <1% of 979 patients were anemia, thrombocytopenia, hepatic dysfunction, renal dysfunction, nausea/vomiting, fever, rash, dyspnea, hemorrhage, infection, stomatitis, somnolence, flu-like syndrome, and edema.

    Tables 5 and 6 present the incidence of selected adverse reactions and laboratory abnormalities reported in patients with various malignancies receiving single agent gemcitabine across 5 clinical trials. Additional clinically significant adverse reactions are provided following Table 6.

    Table 5: Selected Adverse Reactions Occurring in ≥10% of Patients Receiving Single Agent Gemcitabine a


    Adverse ReactionsbGemcitabinec
    All Grades
    (%)
    Grade 3
    (%)
    Grade 4
    (%)
    Nausea and Vomiting 69 13 1
    Fever 41 2 0
    Rash 30 <1 0
    Dyspnea 23 3 <1
    Diarrhea 19 1 0
    Hemorrhage 17 <1 <1
    Infection 16 1 <1
    Alopecia 15 <1 0
    Stomatitis 11 <1 0
    Somnolence 11 <1 <1
    Paresthesias 10 <1 0

    a Grade based on criteria from the World Health Organization (WHO).
    b For approximately 60% of patients, non-laboratory adverse reactions were graded only if assessed to be possibly drug-related. 
    c N=699-974; all patients with laboratory or non-laboratory data.

    Table 6: Selected Laboratory Abnormalities Occurring in Patients Receiving Single Agent Gemcitabine a



    Laboratory AbnormalitybGemcitabinec
    All Grades
    (%)
    Grade 3 (%)Grade 4 (%)
    Hematologic
          Anemia 68 7 1
          Neutropenia 63 19 6
          Thrombocytopenia 24 4 1
    Hepatic
          Increased ALT 68 8 2
          Increased AST 67 6 2
          Increased Alkaline Phosphatase 55 7 2
          Hyperbilirubinemia 13 2 <1
    Renal
          Proteinuria 45 <1 0
          Hematuria 35 <1 0
          Increased BUN 16 0 0
          Increased Creatinine 8 <1 0

    a Grade based on criteria from the WHO.
    b Regardless of causality.
    c N=699-974; all patients with laboratory or non-laboratory data.

    Additional adverse reactions include the following:
    • Transfusion requirements: Red blood cell transfusions (19%); platelet transfusions (<1%)
    • Edema: Edema (13%), peripheral edema (20%) and generalized edema (<1%)
    • Flu-like Symptoms: Fever, asthenia, anorexia, headache, cough, chills, myalgia, asthenia insomnia, rhinitis, sweating, and/or malaise (19%)
    • Infection: Sepsis (<1%)
    • Extravasation: Injection-site reactions (4%)
    • Allergic: Bronchospasm (<2%); anaphylactoid reactions


    Non-Small Cell Lung Cancer
    Tables 7 and 8 presents the incidence of selected adverse reactions and laboratory abnormalities occurring in ≥10% of gemcitabine-treated patients and at a higher incidence in the gemcitabine with cisplatin arm, reported in a randomized trial (Study 3) of gemcitabine with cisplatin (n=260) administered in 28-day cycles as compared to cisplatin alone (n=262) in patients receiving first-line treatment for locally advanced or metastatic non-small cell lung cancer (NSCLC) [see Clinical Studies ( 14.3)].


    Patients randomized to gemcitabine with cisplatin received a median of 4 cycles of treatment and those randomized to cisplatin alone received a median of 2 cycles of treatment. In this trial, the requirement for dose adjustments (>90% versus 16%), discontinuation of treatment for adverse reactions (15% versus 8%), and the proportion of patients hospitalized (36% versus 23%) were all higher for patients receiving gemcitabine with cisplatin compared to those receiving cisplatin alone. The incidence of febrile neutropenia (3% versus <1%), sepsis (4% versus 1%), Grade 3 cardiac dysrhythmias (3% versus <1%) were all higher in the gemcitabine with cisplatin arm compared to the cisplatin alone arm. The two-drug combination was more myelosuppressive with 4 (1.5%) possibly treatment-related deaths, including 3 resulting from myelosuppression with infection and one case of renal failure associated with pancytopenia and infection. No deaths due to treatment were reported on the cisplatin arm.
    Table 7: Selected Adverse Reactions Occurring in ≥10% of Patients Receiving Gemcitabine with Cisplatin and at Higher Incidence than in Patients Receiving Single Agent Cisplatin [Between Arm Difference of ≥5% (All Grades) or ≥2% (Grades 3-4)] in Study 3 a

    Adverse ReactionsbGemcitabine/Cisplatinc
    All Grades
    (%)
    Grade 3 (%)Grade 4 (%)
    Nausea 93 25 2
    Vomiting 78 11 12
    Alopecia 53 1 0
    Neuro Motor 35 12 0
    Diarrhea 24 2 2
    Neuro Sensory 23 1 0
    Infection 18 3 2
    Fever 16 0 0
    Neuro Cortical 16 3 1
    Neuro Mood 16 1 0
    Local 15 0 0
    Neuro Headache 14 0 0
    Stomatitis 14 1 0
    Hemorrhage 14 1 0
    Hypotension 12 1 0
    Rash 11 0 0
    Adverse ReactionsbCisplatind
    All Grades
    (%)
    Grade 3 (%)Grade 4 (%)
    Nausea 87 20 <1
    Vomiting 71 10 9
    Alopecia 33 0 0
    Neuro Motor 15 3 0
    Diarrhea 13 0 0
    Neuro Sensory 18 1 0
    Infection 12 1 0
    Fever 5 0 0
    Neuro Cortical 9 1 0
    Neuro Mood 10 1 0
    Local 6 0 0
    Neuro Headache 7 0 0
    Stomatitis 5 0 0
    Hemorrhage 4 0 0
    Hypotension 7 1 0
    Rash 3 0 0

    a Grade based on National Cancer Institute Common Toxicity Criteria (CTC).
    b Non-laboratory events were graded only if assessed to be possibly drug-related.
    c N=217-253; all Gemcitabine/cisplatin patients with laboratory or non-laboratory data
    d N=213-248; all cisplatin patients with laboratory or non-laboratory data

    Table 8: Selected Laboratory Abnormalities Occurring in >10% of Patients Receiving Gemcitabine with Cisplatin and at Higher Incidence than in Patients Receiving Single Agent Cisplatin [Between Arm Difference of ≥5% (All Grades) or ≥2% (Grades 3-4)] in Study 3 a

    Laboratory AbnormalitybGemcitabine/Cisplatin
    All Grades
    (%)
    Grade 3 (%)Grade 4 (%)
    Hematologic
       Anemia 89 22 3
       Thrombocytopenia 85 25 25
       Neutropenia 79 22 35
       Lymphopenia 75 25 18
       RBC Transfusions e39 - -
       Platelet Transfusions e21 - -
    Hepatic
       Increased Transaminases 22 2 1
       Increased Alkaline 19 1 0
        Phosphatase
    Renal
       Elevated creatinine 38 4 <1
       Proteinuria 23 0 0
       Hematuria 15 0 0
    Other Laboratory Hyperglycemia 30 4 0
       Hypomagnesemia 30 4 3
       Hypocalcemia 18 2 0
    Laboratory AbnormalitybCisplatin
    All GradesGrade 3Grade 4
    (%)(%)(%)
    Hematologic
       Anemia 67 6 1
       Thrombocytopenia 13 3 1
       Neutropenia 20 3 1
       Lymphopenia 51 12 5
       RBC Transfusions e13 - -
       Platelet Transfusions e<1 - -
    Hepatic
       Increased Transaminases 10 1 0
       Increased Alkaline 13 0 0
        Phosphatase
    Renal
       Elevated creatinine 31 2 <1
       Proteinuria 18 0 0
       Hematuria 13 0 0
    Other Laboratory
       Hyperglycemia 23 3 0
       Hypomagnesemia 17 2 0
       Hypocalcemia 7 0 <1

    a Grade based on National Cancer Institute CTC.
    b Regardless of causality.
    c N=217- 253; all gemcitabine plus cisplatin patients with laboratory or non-laboratory data
    d N=213- 248; all cisplatin patients with laboratory or non-laboratory data
    e Percent of patients receiving transfusions. Percent transfusions are not CTC-graded events.

    Tables 9 and 10 present the incidence of selected adverse reactions and laboratory abnormalities occurring in ≥10% of gemcitabine-treated patients and at a higher incidence in the gemcitabine with cisplatin arm, reported in a randomized trial (Study 4) of gemcitabine with cisplatin (n=69) administered in 21-day cycles as compared to etoposide with cisplatin (n=66) in patients receiving first-line treatment for locally advanced or metastatic non-small cell lung cancer (NSCLC) [see Clinical Studies ( 14.3)]. Additional clinically significant adverse reactions are provided following Table 10.


    Patients in the gemcitabine/cisplatin (GC) arm received a median of 5 cycles and those in the etoposide/cisplatin (EC) arm received a median of 4 cycles. The majority of patients receiving more than one cycle of treatment required dose adjustments; 81% in the GC arm and 68% in the EC arm. The incidence of hospitalizations for adverse reactions was 22% in the GC arm and 27% in the EC arm. The proportion of patients who discontinued treatment for adverse reactions was higher in the GC arm (14% versus 8%). The proportion of patients who were hospitalized for febrile neutropenia was lower in the GC arm (7% versus 12%). There was one death attributed to treatment, a patient with febrile neutropenia and renal failure, which occurred in the GC arm.

    Table 9: Selected Adverse Reactions in Patients Receiving Gemcitabine with Cisplatin in Study 4 a

    Adverse ReactionsbGemcitabine/Cisplatinc
    All Grades
    (%)
    Grade 3
    (%)
    Grade 4
    (%)
    Nausea and Vomiting 96 35 4
    Alopecia 77 13 0
    Paresthesias 38 0 0
    Infection 28 3 1
    Stomatitis 20 4 0
    Diarrhea 14 1 1
    Edema e12 - -
    Rash 10 0 0
    Hemorrhage 9 0 3
    Fever 6 0 0
    Somnolence 3 0 0
    Flu-like syndrome e3 - -
    Dyspnea 1 0 1
    Adverse ReactionsbEtoposide/Cisplatind
    All Grades
    (%)
    Grade 3
    (%)
    Grade 4
    (%)
    Nausea and Vomiting 86 19 7
    Alopecia 92 51 0
    Paresthesias 16 2 0
    Infection 21 8 0
    Stomatitis 18 2 0
    Diarrhea 13 0 2
    Edema e2 - -
    Rash 3 0 0
    Hemorrhage 3 0 3
    Fever 3 0 0
    Somnolence 3 2 0
    Flu-like syndrome e0 - -
    Dyspnea 3 0 0

    a Grade based on criteria from the WHO.
    b Non-laboratory events were graded only if assessed to be possibly drug-related. Pain data were not collected.
    c N=67-69; all gemcitabine/cisplatin patients with laboratory or non-laboratory data.
    d N=57-63; all Etoposide/cisplatin patients with laboratory or non-laboratory data.
    e Flu-like syndrome and edema were not graded.

    Table 10: Selected Laboratory Abnormalities Occurring in Patients Receiving Gemcitabine with Cisplatin in Study 4 a

    Laboratory AbnormalitybGemcitabine/Cisplatinc
    All Grades
    (%)
    Grade 3
    (%)
    Grade 4
    (%)
    Hematologic
        Anemia 88 22 0
        Neutropenia 88 36 28
        Thrombocytopenia 81 39 16
        RBC Transfusions c29 - -
        Platelet Transfusions e3 - -
    Hepatic
        Increased Alkaline Phosphatase 16 0 0
        Increased ALT 6 0 0
        Increased AST 3 0 0
        Bilirubin 0 0 0
    Renal
        Hematuria 22 0 0
        Proteinuria 12 0 0
        BUN 6 0 0
        Creatinine 2 0 0
    Laboratory AbnormalitybEtoposlde/Cispatind
    All Grades
    (%)
    Grade 3
    (%)
    Grade 4
    (%)
    Hematologic
        Anemia 77 13 2
        Neutropenia 87 20 56
        Thrombocytopenia 45 8 5
        RBC Transfusions c21 - -
        Platelet Transfusions e8 - -
    Hepatic
        Increased Alkaline Phosphatase 11 0 0
        Increased ALT 12 0 0
        Increased AST 11 0 0
        Bilirubin 0 0 0
    Renal
        Hematuria 10 0 0
        Proteinuria 5 0 0
        BUN 4 0 0
        Creatinine 2 0 0

    a Grade based on criteria from the WHO.
    b Regardless of causality.
    c N=67-69; all gemcitabine/cisplatin patients with laboratory or non-laboratory data.
    d N=57-63; all Etoposide/cisplatin patients with laboratory or non-laboratory data.
    e WHO grading scale not applicable to proportion of patients with transfusions.

    Breast Cancer
    Tables 11 and 12 presents the incidence of selected adverse reactions and laboratory abnormalities, occurring in ≥10% of gemcitabine-treated patients and at a higher incidence in the gemcitabine with paclitaxel arm, reported in a randomized trial (Study 2) of gemcitabine with paclitaxel (n=262) compared to paclitaxel alone (n=259) for the first-line treatment of metastatic breast cancer (MBC) in women who received anthracycline-containing chemotherapy in the adjuvant/neo-adjuvant setting or for whom anthracyclines were contraindicated [see Clinical Studies ( 14.2)]. Additional clinically significant adverse reactions, occurring in <10% of patients, are provided following Table 12.


    The requirement for dose reduction of paclitaxel were higher for patients in the gemcitabine/paclitaxel arm (5% versus 2%). The number of paclitaxel doses omitted (<1%), the proportion of patients discontinuing treatment for adverse reactions (7% versus 5%) and the number of treatment-related deaths (1 patient in each arm) were similar between the two arms.

    Table 11: Selected Adverse Reactions Occurring in Patients Receiving Gemcitabine with Paclitaxel and at Higher Incidence than in Patients Receiving Single Agent Paclitaxel [Between Arm Difference of ≥5% (All Grades) or ≥2%(Grades 3-4)] in Study 2 a

    Adverse ReactionsbGemcitabine/Paclitaxel
    (N=262)
    All Grades
    (%)
    Grade 3
    (%)
    Grade 4
    (%)
    Alopecia 90 14 4
    Neuropathy-sensory 64 5 <1
    Nausea 50 1 0
    Fatigue 40 6 <1
    Vomiting 29 2 0
    Diarrhea 20 3 0
    Anorexia 17 0 0
    Neuropathy-motor 15 2 <1
    Stomatitis/pharyngitis 13 1 <1
    Fever 13 <1 0
    Rash/desquamation 11 <1 <1
    Febrile neutropenia 6 5 <1
    Adverse ReactionsbPaclitaxel
    (N=259)
    All Grades
    (%)
    Grade 3
    (%)
    Grade 4
    (%)
    Alopecia 92 19 3
    Neuropathy-sensory 58 3 0
    Nausea 31 2 0
    Fatigue 28 1 <1
    Vomiting 15 2 0
    Diarrhea 13 2 0
    Anorexia 12 <1 0
    Neuropathy-motor 10 <1 0
    Stomatitis/pharyngitis 8 <1 0
    Fever 3 0 0
    Rash/desquamation 5 0 0
    Febrile neutropenia 2 1 0

    a Grade based on National Cancer Institute CTC Version 2.0.
    b Non-laboratory events were graded only if assessed to be possibly drug-related.
     
    Table 12: Selected Laboratory Abnormalities Occurring in >10% of Patients Receiving Gemcitabine with Paclitaxel and at a Higher Incidence than Patients Receiving Single Agent Paclitaxel [Between Arm Difference of ≥5% (All Grades) or ≥2% (Grades 3-4)] in Study 2 a

    Laboratory AbnormalitybGemcltabine/Paclitaxel
    (N=262)
    All Grades
    (%)
    Grade 3
    (%)
    Grade 4
    (%)
    Hematologic
    Anemia 69 6 1
    Neutropenia 69 31 17
    Thrombocytopenia 26 5 <1
    Hepatobiliary
    Increased ALT 18 5 <1
    Increased AST 16 2 0
    Laboratory AbnormalitybPaclitaxel
    (N=259)
    All Grades
    (%)
    Grade 3
    (%)
    Grade 4
    (%)
    Hematologic
    Anemia 51 3 <1
    Neutropenia 31 4 7
    Thrombocytopenia 7 <1 <1
    Hepatobiliary
    Increased ALT 6 <1 0
    Increased AST 5 <1 0

    a Grade based on National Cancer Institute CTC Version 2.0.
    b Regardless of causality.

    Clinically relevant Grade 3 or 4 dyspnea occurred with a higher incidence in the gemcitabine with paclitaxel arm compared with the paclitaxel arm (1.9% versus 0).

    Ovarian Cancer
    Tables 13 and 14 present the incidence of selected adverse reactions and laboratory abnormalities, occurring in ≥10% of gemcitabine-treated patients and at a higher incidence in the gemcitabine with carboplatin arm, reported in a randomized trial (Study 1) of gemcitabine with carboplatin (n=175) compared to carboplatin alone (n=174) for the second-line treatment of ovarian cancer in women with disease that had relapsed more than 6 months following first-line platinum-based chemotherapy [see Clinical Studies ( 14.1)]. Additional clinically significant adverse reactions, occurring in <10% of patients, are provided following Table 14.


    The proportion of patients with dose adjustments for carboplatin (1.8% versus 3.8%), doses of carboplatin omitted (0.2% versus 0) and discontinuing treatment for adverse reactions (11% versus 10%), were similar between arms. Dose adjustment for gemcitabine occurred in 10% of patients and gemcitabine dose was omitted in 14% of patients in the gemcitabine/carboplatin arm.

    Table 13: Adverse Reactions Occurring in >10% of Patients Receiving in Gemcitabine with Carboplatin and at Higher Incidence than in Patients Receiving Single Agent Carboplatin [Between Arm Difference of ≥5% (All  Grades) or ≥2% (Grades 3-4)] in Study 1 a


    Adverse ReactionsbGemcitabine/Carboplatin (N=175)
    All Grades
    (%)
    Grade
    3(%)
    Grade
    4(%)
    Nausea 69 6 0
    Alopecia 49 0 0
    Vomiting 46 6 0
    Constipation 42 6 1
    Fatigue 40 3 <1
    Diarrhea 25 3 0
    Stomatitis/pharyngitis 22 <1 0
    Adverse ReactionsbCarboplatin
    (N=174)
    All Grades
    (%)
    Grade
    3(%)
    Grade
    4(%)
    Nausea 61 3 0
    Alopecia 17 0 0
    Vomiting 36 2 <1
    Constipation 37 3 0
    Fatigue 32 5 0
    Diarrhea 14 <1 0
    Stomatitis/pharyngitis 13 0 0

    a Grade based on National Cancer Institute CTC Version 2.0.
    b Regardless of causality.

    Table 14: Laboratory Abnormalities Occurring in Patients Receiving Gemcitabine with Carboplatin and at Higher Incidence than in Patients Receiving Single Agent Carboplatin [Between Arm Difference of ≥5% (All Grades) or ≥2% (Grades 3-4)] in Study 1 a


    Laboratory AbnormalitybGemcitabine/Carboplatin
    (N=175)
    All Grades
    (%)
    Grade 3 (%)Grade 4 (%)
    Hematologic
    Neutropenia 90 42 29
    Anemia 86 22 6
    Thrombocytopenia 78 30 5
    RBC Transfusions c38 - -
    Platelet Transfusions c9 - -
    Laboratory AbnormalitybCarboplatin
    (N=174)
    All Grades
    (%)
    Grade 3 (%)Grade 4 (%)
    Hematologic
    Neutropenia 58 11 1
    Anemia 75 9 2
    Thrombocytopenia 57 10 1
    RBC Transfusions c15 - -
    Platelet Transfusions c3 - -

    a Grade based on National Cancer Institute CTC Version 2.0.
    b Regardless of causality.
    c Percent of patients receiving transfusions. Transfusions are not CTC-graded events. Blood transfusions included both packed red blood cells and whole blood.

    Hematopoietic growth factors were administered more frequently in the gemcitabine-containing arm: leukocyte growth factor (24% and 10%) and erythropoiesis-stimulating agent (7% and 3.9%).

    The following clinically relevant Grade 3 and 4 adverse reactions occurred more frequently in the gemcitabine with carboplatin arm: dyspnea (3.4% versus 2.9%), febrile neutropenia (1.1% versus 0), hemorrhagic event (2.3% versus 1.1%), motor neuropathy (1.1% versus 0.6%), and rash/desquamation (0.6% versus 0).

    6.2 Postmarketing Experience

    The following adverse reactions have been identified during post approval use of gemcitabine. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

    • Cardiovascular : Congestive heart failure, myocardial infarction, arrhythmias, supraventricular arrhythmias
    • Vascular : Peripheral vasculitis, gangrene, capillary leak syndrome
    • Skin : Cellulitis, pseudocellulitis, severe skin reactions, including desquamation and bullous skin eruptions
    • Hepatic: Hepatic failure, hepatic veno-occlusive disease
    • Pulmonary: Interstitial pneumonitis, pulmonary fibrosis, pulmonary edema, adult respiratory distress syndrome (ARDS)
    • Nervous System:  Posterior reversible encephalopathy syndrome (PRES)
  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary
    Based on animal data and its mechanism of action, gemcitabine can cause fetal harm when administered to a pregnant woman [see Clinical Pharmacology ( 12.1)]. There are no available data on the use of gemcitabine in pregnant women. In animal reproduction studies, gemcitabine was teratogenic, embryotoxic, and fetotoxic in mice and rabbits (see Data). Advise pregnant women of the potential risk to a fetus [see Use in Special Populations ( 8.3)].

    In the U.S. general population, the estimated background risk of major birth defects and miscarriages in clinically recognized pregnancies 2-4% and 15-20% respectively.

    Data
    Animal Data
    Gemcitabine is embryotoxic in mice. Daily dosing of gemcitabine to pregnant mice increased the incidence of fetal malformation (cleft palate, incomplete ossification) at doses of 1.5 mg/kg/day [approximately 0.005 times the 1000 mg/m 2 clinical dose based on body surface area (BSA)]. Gemcitabine was embryotoxic and fetotoxic in rabbits. Daily dosing of gemcitabine to pregnant rabbits resulted in fetotoxicity (decreased fetal viability, reduced litter sizes, and developmental delays) and increased the incidence of fetal malformations (fused pulmonary artery, absence of gall bladder) at doses of 0.1 mg/kg/day (approximately 0.002 times the 1000 mg/m 2 clinical dose based on BSA).

    8.2 Lactation

    Risk Summary
    There is no information regarding the presence of gemcitabine or its metabolites in human milk, or their effects on the breastfed infant or on milk production. Due to the potential for serious adverse reactions in breastfed infants from gemcitabine, advise women not to breastfeed during treatment with gemcitabine and for at least one week following the last dose.


    8.3 Females and Males of Reproductive Potential

    Pregnancy Testing
    Verify pregnancy status in females of reproductive potential prior to initiating gemcitabine [see Use in Specific Populations ( 8.1)].


    Contraception

    Gemcitabine can cause fetal harm when administered to a pregnant woman [see Use in Specific Populations ( 8.1)].

    Females
    Because of the potential for genotoxicity, advise females of reproductive potential to use effective contraception during treatment with gemcitabine and for 6 months after the final dose of gemcitabine.

    Males
    Because of the potential for genotoxicity, advise males with female partners of reproductive potential to use effective contraception during treatment with gemcitabine and for 3 months after the last dose of gemcitabine [see Nonclinical Toxicology ( 13.1)].


    Infertility

    Males
    Based on animal studies, gemcitabine may impair fertility in males of reproductive potential. It is not known whether these effects on fertility are reversible [see Nonclinical Toxicology ( 13.1)].

    8.4 Pediatric Use

    The safety and effectiveness of gemcitabine have not been established in pediatric patients. The safety and pharmacokinetics of gemcitabine were evaluated in a trial in pediatric patients with refractory leukemia. The maximum tolerated dose was 10 mg/m 2/min for 360 minutes weekly for three weeks followed by a one-week rest period. The safety and activity of gemcitabine were evaluated in a trial of pediatric patients with relapsed acute lymphoblastic leukemia (22 patients) and acute myelogenous leukemia (10 patients) at a dose of 10 mg/m 2/min administered over 360 minutes weekly for three weeks followed by a one-week rest period. Patients with M1 or M2 bone marrow on Day 28 who did not experience unacceptable toxicity were eligible to receive a maximum of one additional four-week course. Toxicities observed included myelosuppression, febrile neutropenia, increased serum transaminases, nausea, and rash/desquamation. No meaningful clinical activity was observed in this trial.

    8.5 Geriatric Use

    In clinical studies which enrolled 979 patients with various malignancies who received single agent gemcitabine, no overall differences in safety were observed between patients aged 65 and older and younger patients, with the exception of a higher rate of Grade 3-4 thrombocytopenia in older patients as compared to younger patients.
    In a randomized trial in women with ovarian cancer (Study 1), 175 women received gemcitabine with carboplatin, of which 29% were age 65 years or older. Similar effectiveness was observed between older and younger women. There was significantly higher Grade 3-4 neutropenia in women 65 years of age or older [see Dosage and Administration ( 2.1)].

    Gemcitabine clearance is affected by age; however, there are no recommended dose adjustments based on patients' age [see Clinical Pharmacology (12.3)] .

    8.6 Gender

    Gemcitabine  clearance is decreased in females [see Clinical Pharmacology (12.3)]. In single agent studies of gemcitabine, women, especially older women, were more likely not to proceed to a subsequent cycle and to experience Grade 3-4 neutropenia and thrombocytopenia [see Dosage and Administration ( 2.1, 2.2. 2.3, 2.4)].

  • 10 OVERDOSAGE

    There is no known antidote for overdoses of gemcitabine. Myelosuppression, paresthesias, and severe rash were the principal toxicities seen when a single dose as high as 5,700 mg/m 2 was administered by intravenous infusion over 30 minutes every 2 weeks to several patients in a dose-escalation study. In the event of suspected overdose, monitor with appropriate blood counts and provide supportive therapy, as necessary.

  • 11 DESCRIPTION

    Gemcitabine is a nucleoside metabolic inhibitor. Gemcitabine hydrochloride is 2′-deoxy-2′, 2′-difluorocytidine monohydrochloride (β-isomer) with the following structural formula:






    Structural Formula


    The empirical formula for gemcitabine hydrochloride is C 9H 11F 2N 3O 4 • HCl. It has a molecular weight of 299.66 g/mol.

    Gemcitabine hydrochloride is soluble in water, slightly soluble in methanol, and practically insoluble in ethanol and polar organic solvents.

    Gemcitabine for Injection, USP is a sterile white to off-white lyophilized powder or cake and available as 200 mg and 1 g single-dose vials for intravenous use only. Each 200 mg vial contains 200 mg gemcitabine hydrochloride (expressed as free base), 200 mg mannitol and 12.5 mg sodium acetate. Each 1 g vial contains 1 g gemcitabine hydrochloride (expressed as free base), 1 g mannitol, and 62.5 mg sodium acetate. Hydrochloric acid and/or sodium hydroxide may have been added for pH adjustment.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Gemcitabine kills cells undergoing DNA synthesis and blocks the progression of cells through the G1/S-phase boundary. Gemcitabine is metabolized by nucleoside kinases to diphosphate (dFdCDP) and triphosphate (dFdCTP) nucleosides. Gemcitabine diphosphate inhibits ribonucleotide reductase, an enzyme responsible for catalyzing the reactions that generate deoxynucleoside triphosphates for DNA synthesis, resulting in reductions in deoxynucleotide concentrations, including dCTP. Gemcitabine triphosphate competes with dCTP for incorporation into DNA. The reduction in the intracellular concentration of dCTP by the action of the diphosphate enhances the incorporation of gemcitabine triphosphate into DNA (self-potentiation). After the gemcitabine nucleotide is incorporated into DNA, only one additional nucleotide is added to the growing DNA strands, which eventually results in the initiation of apoptotic cell death.

    12.3 Pharmacokinetics

    The pharmacokinetics of gemcitabine were examined in 353 patients with various solid tumors. Pharmacokinetic parameters were derived using data from patients treated for varying durations of therapy given weekly with periodic rest weeks and using both short infusions (<70 minutes) and long infusions (70 to 285 minutes). The total gemcitabine dose varied from 500 mg/m 2 to 3,600 mg/m 2.

    Distribution
    The volume of distribution was increased with infusion length. Volume of distribution of gemcitabine was 50 L/m 2 following infusions lasting <70 minutes. For long infusions, the volume of distribution rose to 370 L/m 2.

    Gemcitabine pharmacokinetics are linear and are described by a 2-compartment model. Population pharmacokinetic analyses of combined single and multiple dose studies showed that the volume of distribution of gemcitabine was significantly influenced by duration of infusion and sex. Gemcitabine plasma protein binding is negligible.

    Elimination
    Metabolism
    The active metabolite, gemcitabine triphosphate, can be extracted from peripheral blood mononuclear cells. The half-life of the terminal phase for gemcitabine triphosphate from mononuclear cells ranges from 1.7 to 19.4 hours.

    Excretion
    Gemcitabine disposition was studied in 5 patients who received a single 1,000 mg/m 2 of radiolabeled drug as a 30-minute infusion. Within one week, 92% to 98% of the dose was recovered, almost entirely in the urine. Gemcitabine (<10%) and the inactive uracil metabolite, 2´-deoxy-2´, 2´-difluorouridine (dFdU) accounted for 99% of the excreted dose. The metabolite dFdU is also found in plasma.

    Specific Populations
    Geriatric Patients
    Clearance of gemcitabine was affected by age. The lower clearance in geriatric patients results in higher concentrations of gemcitabine for any given dose. Differences in either clearance or volume of distribution based on patient characteristics or the duration of infusion result in changes in half-life and plasma concentrations. Table 15 shows plasma clearance and half-life of gemcitabine following short infusions for typical patients by age and gender.

    Table 15: Gemcitabine Clearance and Half-Life for the “Typical” Patient


    AgeClearance
    Men
    (L/hr/m2)
    Clearance
    Women
    (L/hr/m2)
    Half-Life a
    Men
    (min)
    Half-Life a
    Women
    (min)
    29 92.2 69.4 42 49
    45 75.7 57.0 48 57
    65 55.1 41.5 61 73
    79 40.7 30.7 79 94

    a Half-life for patients receiving a <70 minute infusion.
    Gemcitabine half-life for short infusions ranged from 42 to 94 minutes and for long infusions varied from 245 to 638 minutes, depending on age and gender, reflecting a greatly increased volume of distribution with longer infusions.

    Male and Female Patients
    Females have lower clearance and longer half-lives than male patients as described in Table 15.

    Patients with Renal Impairment
    No clinical studies have been conducted with gemcitabine in patients with decreased renal function.

    Patients with Hepatic Impairment
    No clinical studies have been conducted with gemcitabine in patients with decreased hepatic function.

    Drug Interaction Studies
    When gemcitabine (1,250 mg/m 2 on Days 1 and 8) and cisplatin (75 mg/m 2 on Day 1) were administered in patients with NSCLC, the clearance of gemcitabine on Day 1 was 128 L/hr/m 2 and on Day 8 was 107 L/hr/m 2. Data from patients with NSCLC demonstrate that gemcitabine and carboplatin given in combination does not alter the pharmacokinetics of gemcitabine or carboplatin compared to administration of either single agent; however, due to wide confidence intervals and small sample size, interpatient variability may be observed.

    Data from metastatic breast cancer patients shows that gemcitabine has little or no effect on the pharmacokinetics (clearance and half-life) of paclitaxel and paclitaxel has little or no effect on the pharmacokinetics of gemcitabine.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Long-term animal studies to evaluate the carcinogenic potential of gemcitabine have not been conducted. Gemcitabine was mutagenic in an in vitro mouse lymphoma (L5178Y) assay and was clastogenic in an in vivo mouse micronucleus assay. Gemcitabine intraperitoneal doses of 0.5 mg/kg/day [about 1/700 the 1,000 mg/m 2 clinical dose based on body surface area (BSA)] in male mice resulted in moderate to severe hypospermatogenesis, decreased fertility, and decreased implantations. In female mice, fertility was not affected but maternal toxicities were observed at 1.5 mg/kg/day administered intravenously (about 1/200 the 1,000 mg/m 2 clinical dose based on BSA) and fetotoxicity or embryolethality was observed at 0.25 mg/kg/day administered intravenously (about 1/1,300 the 1,000 mg/m 2 clinical dose based on BSA).

  • 14 CLINICAL STUDIES

    14.1 Ovarian Cancer

    The efficacy of gemcitabine was evaluated in a randomized trial (Study 1) conducted in women with advanced ovarian cancer that had relapsed at least 6 months after first-line platinum-based therapy. Patients were randomized to receive either gemcitabine 1,000 mg/m 2 on Days 1 and 8 of each 21-day cycle with carboplatin AUC 4 on Day 1 after gemcitabine administration (n=178) or carboplatin AUC 5 on Day 1 of each 21-day cycle (n=178). The major efficacy outcome measure was progression free survival (PFS).

    A total of 356 patients were enrolled. Demographics and baseline characteristics are shown in Table 16.

    Efficacy results are presented in Table 17 and Figure 1. The addition of gemcitabine to carboplatin resulted in statistically significant improvements in PFS and overall response rate. Approximately 75% of patients in each arm received additional chemotherapy for disease progression; 13 of 120 patients in the carboplatin alone arm received gemcitabine for treatment of disease progression. There was no significant difference in overall survival between the treatment arms.


    Table 16: Baseline Demographics and Clinical Characteristics for Study 1

    Gemcitabine/
    Carboplatin (N = 178)
    Carboplatin (N = 178)
    Median age, years 59 58
          Range 36 to 78 21 to 81
    Baseline ECOG performance status 0-1 a94% 95%
    Disease Status
          Evaluable 8% 3%
          Bidimensionally measurable 92% 96%
    Platinum-free interval b
          6-12 months 40% 40%
          >12 months 59% 60%
    First-line therapy
          Platinum-taxane combination 70% 71%
          Platinum-non-taxane
            combination
    29% 28%
          Platinum monotherapy 1% 1%

    a 5 patients on Gemcitabine with carboplatin arm and 4 patients on carboplatin arm had no baseline Eastern Cooperative Oncology Group (ECOG) performance status.
    b 2 patients on Gemcitabine with carboplatin arm and 1 patient on carboplatin arm had platinum-free interval <6 months.

    Table 17: Efficacy Results in Study 1

    Efficacy ParameterGemcitabine/ Carboplatin (N = 178)Carboplatin (N = 178)
    Progression-free Survival
          Median (95% Cl a) in months 8.6 (8.0, 9.7) 5.8 (5.2, 7.1)
          Hazard Ratio (95% Cl) 0.72 (0.57, 0.90)
          p-value bp=0.0038
    Overall Survival
          Median (95% Cl) in months 18.0 (16.2, 20.3) 17.3 (15.2,19.3)
          Hazard Ratio (95% Cl) 0.98 (0.78, 1.24)
          p-value bp=0.8977
    Overall Response Rate by Investigator Review47.2% 30.9%
          p-value cp=0.0016
          CR d14.6% 6.2%
          PR with PRNM e32.6% 24.7%
    Overall Response Ratef by Independent Review46.3% 35.6%
          p-value cp=0.11
          CR d9.1% 4.0%
          PR with PRNM e37.2% 31.7%

    aCI=confidence interval.
    bLog rank, unadjusted.
    cChi square.
    dCR=Complete response.
    ePR with PRNM=Partial response with partial response, non-measurable disease.
    fIndependently reviewed cohort - gemcitabine/carboplatin (n=121), carboplatin (n=101); independent reviewers unable to measure disease detected by sonography or physical exam.

    Figure 1: Kaplan-Meier Curves for Progression Free Survival in Study 1



    gr-1

    14.2 Breast Cancer

    The efficacy of gemcitabine were evaluated in a multi-national, randomized, open-label trial (Study 2) conducted in women receiving initial treatment for metastatic breast cancer and who have received prior adjuvant/neoadjuvant anthracycline chemotherapy unless clinically contraindicated. Patients were randomized to receive either gemcitabine 1,250 mg/m 2 on Days 1 and 8 of each 21-day cycle with paclitaxel 175 mg/m 2 administered on Day 1 before gemcitabine administration (n=267) or paclitaxel 175 mg/m 2 on Day 1 of each 21-day cycle (n=262). The major efficacy outcome measure was time to documented disease progression.

    A total of 529 patients were enrolled. Demographic and baseline characteristics were similar between treatment arms (Table 18).


    Efficacy results are presented in Table 19 and Figure 2. The addition of gemcitabine to paclitaxel resulted in statistically significant improvement in time to documented disease progression and overall response rate compared to paclitaxel alone. There was no significant difference in overall survival.


    Table 18: Baseline Demographics and Clinical Characteristics for Study 2




    Gemcitabine/ Paclitaxel (N = 267)Paclitaxel (N = 262)
    Median age (years) 53 52
          Range 26 to 83 26 to 75
    Metastatic disease 97% 97%
    Baseline KPS a ≥90 70% 74%
    Number of tumor sites
          1 -2 57% 59%
          ≥3 43% 41%
    Visceral disease 73% 73%
    Prior anthracycline 97% 96%


    a Karnofsky Performance Status.

    Table 19: Efficacy Results in Study 2


    Efficacy ParameterGemcitabine/
    Paclitaxel
    (N=267)
    Paclitaxel
    (N=262)
    Time to Documented Disease Progression a
          Median (95% Cl) in months 5.2 (4.2, 5.6) 2.9 (2.6, 3.7)
          Hazard Ratio (95% Cl) 0.650 (0.59, 0.85)
          p-value p<0.0001
    Overall Survivalb
          Median (95% Cl) in months 18.6 (16.6,20.7) 15.8 (14.1,17.4)
          Hazard Ratio (95% Cl) 0.86 (0.71,1.04)
          p-value Not Significant
    Overall Response Rate40.8% 22.1%
          (95% Cl) (34.9, 46.7) (17.1,27.2)
          p-value p<0.0001

    a These represent reconciliation of investigator and Independent Review Committee assessments according to a predefined 
      algorithm.
    b Based on the ITT population.

    Figure 2: Kaplan-Meier Curves for Time to Documented Disease Progression in Study 2



    gr-2

    14.3 Non-Small Cell Lung Cancer (NSCLC)

    The efficacy of gemcitabine was evaluated in two randomized, multicenter trials.

    Study 3: 28-Day Schedule
    A multinational, randomized trial (Study 3) compared gemcitabine with cisplatin to cisplatin alone in the treatment of patients with inoperable Stage IIIA, IIIB, or IV NSCLC who had not received prior chemotherapy. Patients were randomized to receive either gemcitabine 1,000 mg/m 2 on Days 1, 8, and 15 of each 28-day cycle with cisplatin 100 mg/m 2 on Day 1 after gemcitabine administration (N=260) or cisplatin 100 mg/m 2 on Day 1 of each 28-day cycle (N=262). The major efficacy outcome measure was overall survival.

    A total of 522 patients were enrolled. Demographics and baseline characteristics (Table 20) were similar between arms with the exception of histologic subtype of NSCLC, with 48% of patients on the cisplatin arm and 37% of patients on the gemcitabine with cisplatin arm having adenocarcinoma.

    Efficacy results are presented in Table 21 and Figure 3.

    Study 4: 21-Day Schedule
    A randomized (1:1), multicenter trial (Study 4) was conducted in patients with Stage IIIB or IV NSCLC. Patients were randomized to receive either gemcitabine 1,250 mg/m 2 on Days 1 and 8 of each 21-day cycle with cisplatin 100 mg/m 2 on Day 1 after gemcitabine administration or etoposide 100 mg/m 2 intravenously on Days 1, 2, and 3 with cisplatin 100 mg/m 2 on Day 1 of each 21-day cycle. The major efficacy outcome measure was response rate.

    A total of 135 patients were enrolled. Demographics and baseline characteristics are summarized in Table 20.

    Efficacy results are presented in Table 21. There was no significant difference in survival between the two treatment arms. The median survival was 8.7 months for the gemcitabine with cisplatin arm versus 7 months for the etoposide with cisplatin arm. Median time to disease progression for the gemcitabine with cisplatin arm was 5 months compared to 4.1 months on the etoposide with cisplatin arm (Log rank p=0.015, two-sided). The objective response rate for the gemcitabine with cisplatin arm was 33% compared to 14% on the etoposide with cisplatin arm (Fisher's Exact p=0.01, two-sided).



    Table 20: Baseline Demographics and Clinical Characteristics for Studies 3 and 4

    Trial28-day Schedule (Study 3)21-day Schedule (Study 4)
    Gemcitabine/ Cisplatin
    (N = 260)
    Cisplatin
    (N = 262)
    Gemcitabine/ Cisplatin
    (N = 69)
    Etoposide/Cisplatin
    (N = 66)
    Male 70% 71% 93% 92%
    Median age, years 62 63 58 60
    Range 36 to 88 35 to 79 33 to 76 35 to 75
    Stage IIIA 7% 7% N/A aN/A a
    Stage II IB 26% 23% 48% 52%
    Stage IV 67% 70% 52% 49%
    Baseline KPS b
    70 to 80
    41% 44% 45% 52%
    Baseline KPS b
    90 to 100
    57% 55% 55% 49%

    N/A Not applicable.
    b Karnofsky Performance Status.


    Table 21: Efficacy Results for Studies 3 and 4


    Trial28-day Schedule (Study 3)21 -day Schedule (Study 4)
    Efficacy ParameterGemcitabine/
    Cisplatin
    (N = 260)
    Cisplatin
    (N=262)
    Gemcitabine/
    Cisplatin
    (N=69)
    Etoposide/
    Cisplatin
    (N=66)
    Survival
          Median (95% Cl a) in months 9.0
    (8.2, 11.0)
    7.6
    (6.6, 8.8)
    8.7
    (7.8, 10.1)
    7.0
    (6.0, 9.7)
          p-value bp=0.008 p=0.18
    Time to Disease Progression
          Median (95% Cl a) in months 5.2
    (4.2, 5.7)
    3.7
    (3.0, 4.3)
    5.0
    (4.2, 6.4)
    4.1
    (2.4, 4.5)
          p-value bp=0.009 p=0.05
    Tumor Response26% 10% 33% 14%
          p-value bp<0.0001 p=0.01

    a CI=confidence intervals.
    b p-value two-sided Fisher’s Exact test for difference in binomial proportions; log rank test for time-to-event analyses.

    Figure 3: Kaplan-Meier Curves for Overall Survival in Study 3


    fig-3

    14.4 Pancreatic Cancer


    The efficacy of gemcitabine was evaluated in two trials (Studies 5 and 6), a randomized, single-blind, two-arm, active-controlled trial (Study 5)conducted in patients with locally advanced or metastatic pancreatic cancer who had received no prior chemotherapy and in a single-arm, open-label, multicenter trial (Study 6)conducted in patients with locally advanced or metastatic pancreatic cancer previously treated with fluorouracil or a fluorouracil-containing regimen. In Study 5, patients were randomized to receive either gemcitabine 1,000 mg/m 2 intravenously over 30 minutes once weekly for 7 weeks followed by a one-week rest, then once weekly for 3 consecutive weeks every 28-days in subsequent cycles (n=63) or fluorouracil 600 mg/m 2 intravenously over 30 minutes once weekly (n=63). In Study 6, all patients received gemcitabine 1,000 mg/m 2 intravenously over 30 minutes once weekly for 7 weeks followed by a one-week rest, then once weekly for 3 consecutive weeks every 28-days in subsequent cycles.


    The major efficacy outcome measure in both trials was "clinical benefit response". A patient was considered to have had a clinical benefit response if either of the following occurred:
    • The patient achieved a ≥50% reduction in pain intensity (Memorial Pain Assessment Card) or analgesic consumption, or a 20-point or greater improvement in performance status (Karnofsky Performance Status) for a period of at least 4 consecutive weeks, without showing any sustained worsening in any of the other parameters. Sustained worsening was defined as 4 consecutive weeks with either any increase in pain intensity or analgesic consumption or a 20-point decrease in performance status occurring during the first 12 weeks of therapy.
    OR
    • The patient was stable on all of the aforementioned parameters and showed a marked, sustained weight gain (≥7% increase maintained for ≥4 weeks) not due to fluid accumulation.
    Study 5 enrolled 126 patients. Demographics and baseline characteristics were similar between the arms (Table 22). The efficacy results are shown in Table 23 and Figure 4. Patients treated with gemcitabine had statistically significant increases in clinical benefit response, survival, and time to disease progression compared to those randomized to receive fluorouracil. No confirmed objective tumor responses were observed in either treatment arm.

    Table 22: Baseline Demographics and Clinical Characteristics for Study 5

    Gemcitabine
    (N=63)
    Fluorouracil
    (N=63)
    Male 54% 54%
    Median age 62 years 61 years
    Range 37 to 79 36 to 77
    Stage IV disease 71% 76%
    Baseline KPS a≤70 70% 68%

    a Karnofsky Performance Status.


    Table 23: Efficacy Results in Study 5


    Efficacy ParameterGemcitabine
    (N=63)
    Fluorouracil
    (N=63)
    Clinical benefit response22.2% 4.8%
    p-value ap=0.004
    Overall Survival
    Median (95% Cl) in months 5.7 (4.7, 6.9) 4.2 (3.1,5.1)
    p-value ap=0.0009
    Time to Disease Progression
    Median (95% Cl) in months 2.1 (1.9, 3.4) 0.9 (0.9,1.1)
    p-value ap=0.0013

    a p-value for clinical benefit response calculated using the two-sided test for difference in binomial proportions. All other p-values are calculated using log rank test.


    Figure 4: Kaplan-Meier Curves for Overall Survival in Study 5



    gr-4



  • 15 REFERENCES

    1. OSHA Hazardous Drugs.” OSHA.
     http://www.osha.gov/SLTC/hazardousdrugs/index.html


  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    Gemcitabine for Injection, USP is a sterile white to off-white lyophilized powder or cake available in single-dose vials individually packaged in a carton containing 200 mg or 1 g gemcitabine:

    Product CodeUnit of SaleStrength
    PRX101210 NDC 63323-102-94
    Individually packaged
    200 mg per vial
    PRX102550 NDC 63323-125-94
    Individually packaged
    1 gram per vial

    Gemcitabine for Injection, USP is a cytotoxic drug. Follow applicable special handling and disposal procedures. 1
    Store at controlled room temperature 20ºC to 25ºC (68ºF to 77ºF); excursions permitted between 15ºC and 30ºC (59ºF and 86ºF) [see USP Controlled Room Temperature].

    The container closure is not made with natural rubber latex.

  • 17 PATIENT COUNSELING INFORMATION

    Myelosuppression
    Advise patients of the risks of myelosuppression. Instruct patients to immediately contact their healthcare provider should any signs or symptoms of infection, including fever, or if bleeding or signs of anemia, occur [see Warnings and Precautions ( 5.2)].

    Pulmonary Toxicity
    Advise patients of the risks of pulmonary toxicity, including respiratory failure and death. Instruct patients to immediately contact their healthcare provider for development of shortness of breath, wheezing, or cough [see Warnings and Precautions ( 5.3)].

    Hemolytic-Uremic Syndrome and Renal Failure
    Advise patients of the risks of hemolytic-uremic syndrome and associated renal failure. Instruct patients to immediately contact their healthcare provider for changes in the color or volume of urine output or for increased bruising or bleeding [see Warnings and Precautions ( 5.4)].

    Hepatic Toxicity
    Advise patients of the risks of hepatic toxicity including liver failure and death. Instruct patients to immediately contact their healthcare provider for signs of jaundice or for pain/tenderness in the right upper abdominal quadrant [see Warnings and Precautions ( 5.5)].

    Embryo-Fetal Toxicity
    Advise females and males of reproductive potential that gemcitabine can cause fetal harm. Advise females of reproductive potential to use effective contraception during treatment with gemcitabine and for 6 months after the final dose. Advise male patients with female partners of reproductive potential to use effective contraception during treatment with gemcitabine and for 3 months after the final dose [see Warnings and Precaution ( 5.6), Use in Specific Populations ( 8.1, 8.3)].

    Lactation
    Advise women not to breastfeed during treatment with gemcitabine and for at least one week after the last dose [see Use in Specific Populations ( 8.2)].

    Infertility
    Advise males of reproductive potential of the potential for reduced fertility with gemcitabine [see Use in Specific Populations ( 8.3), Nonclinical Toxicology ( 13.1)].

    PREMIERProRx ® is a registered trademark of Premier Healthcare Alliance, L.P., used under license.

    Manufactured by:
    Fresenius Kabi
    Lake Zurich, IL 60047

    For Product Inquiry:
    1-800-551-7176 or www.fresenius-kabi.com/us

    451331 /Issued: June 2019

    PREMIERPro Logo

  • PACKAGE LABEL - PRINCIPAL DISPLAY PANEL - Gemcitabine 200mg-Vial Carton


    NDC: 63323-102-94     PRX101210


    GEMCITABINE 
    FOR INJECTION, USP
    200 mg per vial


    For Intravenous use only
    Must Be Diluted 




    DO NOT REFRIGERATE
    Cytotoxic Agent
    Rx only
    Single-Dose Vial



    200mg



    PRINCIPAL DISPLAY PANEL- Gemcitabine for Injection, 200 mg- Vial Label


    NDC: 63323-102-94     PRX101210


    GEMCITABINE 
    FOR INJECTION, USP
    200 mg per vial


    For Intravenous use only
    Must Be Diluted 




    Rx only
    Single-Dose Vial


    vial-200mg


  • PACKAGE LABEL - PRINCIPAL DISPLAY PANEL - Gemcitabine 1g-Vial Carton

    NDC 63323-125-94      PRX102550

    GEMCITABINE
    FOR INJECTION, USP
    1 g per vial

    For Intravenous use only
    Must Be Diluted

    DO NOT REFRIGERATE
    Cytotoxic Agent
    Rx only
    Single-Dose Vial



    carton-1g

    PRINCIPAL DISPLAY PANEL- Gemcitabine for Injection, 1 g- Vial Label
    NDC 63323-125-94      PRX102550

    GEMCITABINE
    FOR INJECTION, USP
    1 g per vial

    For Intravenous use only
    Must Be Diluted

    Rx only
    Single-Dose Vial



    vial-1g
  • INGREDIENTS AND APPEARANCE
    GEMCITABINE 
    gemcitabine injection, powder, lyophilized, for solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:63323-102
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GEMCITABINE HYDROCHLORIDE (UNII: U347PV74IL) (GEMCITABINE - UNII:B76N6SBZ8R) GEMCITABINE200 mg  in 5.26 mL
    Inactive Ingredients
    Ingredient NameStrength
    MANNITOL (UNII: 3OWL53L36A)  
    SODIUM ACETATE (UNII: 4550K0SC9B)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63323-102-941 in 1 BOX07/26/2011
    15.26 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA09079907/26/2011
    GEMCITABINE  
    gemcitabine injection, powder, lyophilized, for solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:63323-125
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GEMCITABINE HYDROCHLORIDE (UNII: U347PV74IL) (GEMCITABINE - UNII:B76N6SBZ8R) GEMCITABINE1 g  in 26.3 mL
    Inactive Ingredients
    Ingredient NameStrength
    MANNITOL (UNII: 3OWL53L36A)  
    SODIUM ACETATE (UNII: 4550K0SC9B)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63323-125-941 in 1 BOX07/26/2011
    126.3 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA09079907/26/2011
    Labeler - Fresenius Kabi USA, LLC (608775388)
    Establishment
    NameAddressID/FEIBusiness Operations
    Fresenius Kabi USA, LLC023648251manufacture(63323-102, 63323-125)
    Establishment
    NameAddressID/FEIBusiness Operations
    Fresenius Kabi Oncology Limited677601939manufacture(63323-102, 63323-125)