Label: THROMBATE III (antithrombin iii- human kit

  • NDC Code(s): 13533-000-05, 13533-100-50, 13533-200-10, 13533-602-50, view more
    13533-603-20, 13533-604-25, 13533-605-21
  • Packager: GRIFOLS USA, LLC
  • Category: PLASMA DERIVATIVE
  • DEA Schedule: None
  • Marketing Status: Biologic Licensing Application

Drug Label Information

Updated January 25, 2019

If you are a consumer or patient please visit this version.

  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use THROMBATE III safely and effectively. See full prescribing information for THROMBATE III. 

    THROMBATE III [Antithrombin III (Human)]
    Lyophilized Powder for Solution for Intravenous Injection

    Initial U.S. Approval: 1991

    INDICATIONS AND USAGE

    THROMBATE III is a human antithrombin (AT) indicated in patients with hereditary antithrombin deficiency for:

    • Treatment and prevention of thromboembolism
    • Prevention of peri-operative and peri-partum thromboembolism (1)

    DOSAGE AND ADMINISTRATION

    For intravenous use after reconstitution only

    • Individualize dose to achieve AT level of 80% to 120% of normal human plasma (2.1)
    DoseTarget AT
    Level
    Dose (Units)Monitor AT Level 
    Loading120% of normal120 % - baseline x body weight(kg)
    divided by 1.4%
    • baseline
    • 20 minutes (peak) post-injection
    • 12 hours post-injection
    • pre-injection (trough)
    Adjustment
    (as needed)
    80% to 120% of normal Target % - trough % x body weight (kg)
    divided by 1.4%
    • 20 minutes (peak) post-injection
    • at least every 12 hours post-injection
    • pre-injection (trough)
    Maintenance
    (every 24 hours, as needed)
    80% to 120% of normal Loading Dose x 0.6
    • approximately every 24 hours, as needed

    Adapt the rate of administration to the response of the patient; typically the full dose is given over 10 to 20 minutes.  (2.3)

    DOSAGE FORMS AND STRENGTHS

    For injection: approximately 500 units, lyophilized powder in single-use vial for reconstitution. (3)

    CONTRAINDICATIONS

    None. (4)

    WARNINGS AND PRECAUTIONS

    • Hypersensitivity reactions, including anaphylaxis, are possible.  Should symptoms occur, discontinue THROMBATE III infusion and begin appropriate treatment. (5.1)
    • Because THROMBATE III is made from human blood, it may carry a risk of transmitting infectious agents, e.g., viruses, the variant Creutzfeldt-Jakob disease (vCJD) agent and, theoretically, the Creutzfeldt-Jakob (CJD) disease agent. (5.2)
    • Perform coagulation tests to avoid excessive or insufficient anticoagulation and monitor for bleeding or thrombosis. Measure functional plasma AT levels with amidolytic or clotting assays; do not use immunoassays. (5.3)

    ADVERSE REACTIONS

    The most common adverse reactions (≥ 5% of subjects) in clinical studies were dizziness, chest discomfort, nausea, dysgeusia, and pain (cramps). (6)

    To report SUSPECTED ADVERSE REACTIONS, contact Grifols Therapeutics LLC at 1-800-520-2807 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    DRUG INTERACTIONS

    The anticoagulant effect of heparin is enhanced by concurrent treatment with THROMBATE III. To avoid bleeding, reduce the dosage of heparin. (7)

    USE IN SPECIFIC POPULATIONS

    Pregnancy: suspend heparin administration and continue THROMBATE III administration during labor and delivery. (8.1)

    See 17 for PATIENT COUNSELING INFORMATION.

    Revised: 1/2019

  • Table of Contents
  • 1 INDICATIONS AND USAGE

    THROMBATE III is a human antithrombin (AT) indicated in patients with hereditary antithrombin deficiency for:

    • Treatment and prevention of thromboembolism
    • Prevention of peri-operative and peri-partum thromboembolism
  • 2 DOSAGE AND ADMINISTRATION

    For intravenous use after reconstitution only

    2.1 Dose

    • Each vial of THROMBATE III has the functional activity, in International Units (units), stated on the label of the vial. The potency assignment has been determined with a standard calibrated against a World Health Organization antithrombin reference preparation. When prepared as directed, the approximate final concentration is 50 units per milliliter.
    • A guide for dosing THROMBATE III is provided in Table 1.
    Table 1: Dosing Guidelines
    *
    The dose calculation is based on an expected incremental in vivo recovery of 1.4% per unit per kilogram above baseline or trough levels.
    Expressed as % normal level based on functional AT assay.
    Regimen
    (timing)
    Target AT
    Level
    Dose (Units)Monitor AT Level 
    Loading Dose*120% of normal120 % - baseline %  x  body weight (kg)
    1.4%
    • baseline
    • 20 minutes (peak) post-injection
    • 12 hours post-injection
    • pre-injection (trough)
    Dose Adjustment*
    (adjust as needed)
    80% to 120% of normalTarget % - trough %  x  body weight (kg)
    1.4%
    • 20 minutes (peak) post-injection
    • at least every 12 hours post-injection
    • pre-injection (trough)
    Maintenance
    Dose
    (approximately
    every 24 hours,
    adjust as needed)
    80% to 120% of normalLoading Dose x 0.6
    • approximately every 24 hours, as needed
    • Monitor functional plasma levels of AT. [see table above and Warnings and Precautions (5.3)] and adjust subsequent dosing based on the trough level achieved with the preceding dose until predictable peak and trough levels have been achieved, generally between 80% to 120% of normal.(1)
    • Maintain plasma AT levels between 80% to 120% by administering maintenance doses of 60% of the loading dose, administered every 24 hours. Adjust the maintenance dose and interval between doses based on actual plasma AT levels achieved.
    • Individualize the exact loading and maintenance dose and/or dose intervals for each patient based on the individual clinical conditions, response to therapy, and actual plasma AT levels achieved. Recovery of THROMBATE III may vary by patient. For example,
      • The half-life of AT has been reported to be shortened following surgery,(2) hemorrhage or acute thrombosis, and during intravenous heparin (or low molecular weight heparin) administration.(3-6) In such conditions, monitor plasma AT levels more frequently, and administer THROMBATE III as necessary. [see Warnings and Precautions (5.3),Drug Interactions (7)]
      • When an infusion of THROMBATE III is indicated for a patient with hereditary deficiency to control an acute thrombotic episode or prevent thrombosis during or following surgical or obstetrical procedures, raise the AT level to normal and maintain this level for 2 to 8 days, depending on the indication for treatment, type and extent of surgery, patient’s medical condition, past history and physician’s judgment. Base the concomitant administration of heparin in each of these situations on the medical judgment of the physician. [see Drug Interactions (7)]

    2.2 Reconstitution

    1. Warm THROMBATE III and Sterile Water for Injection, USP (diluent) vials to room temperature before reconstitution.
    2. Remove shrink band from the THROMBATE III vial. If the shrink band is absent or shows signs of tampering, do not use the product and notify Grifols Therapeutics LLC immediately.
    3. Remove the plastic flip top from each vial (Fig. A). Cleanse each vial stopper with an alcohol swab and allow surface to dry.
    4. Carefully remove the plastic sheath from the short end of the transfer needle. Insert the exposed needle into the diluent vial to the hub (Fig. B).
    5. Carefully grip the sheath of the other end of the transfer needle and twist to remove it.
    6. Invert the diluent vial and insert the attached needle into the THROMBATE III vial at a 45° angle (Fig. C). This will direct the stream of diluent against the wall of the vial and minimize foaming. The vacuum will draw the diluent into the THROMBATE III vial.*
    7. When diluent transfer is complete, remove the diluent vial and transfer needle (Fig. D).
    8. Immediately after adding the diluent, swirl the THROMBATE III vial continuously until the product is completely dissolved (Fig. E). Some foaming may occur, but attempt to avoid excessive foaming. Visually inspect the vial for particulate matter and discoloration prior to administration.
    9. Clean the top of the vial of reconstituted THROMBATE III again with a new alcohol swab and let surface dry.
    10. Attach the filter needle (from the package) to the sterile syringe. Withdraw the THROMBATE III solution into the syringe through the filter needle (Fig. F).
    11. Remove the filter needle from the syringe and replace with an appropriate injection or butterfly needle for administration.
    12. If the same patient is using more than one vial of THROMBATE III, draw the contents of multiple vials into the same syringe through the filter needles provided.
    *
    If vacuum is lost in the THROMBATE III vial during reconstitution, use a sterile syringe to remove the sterile water from the diluent vial and inject it into the THROMBATE III vial, directing the stream of fluid against the wall of the vial.
    Figures

    2.3 Administration

    • Visually inspect parenteral drug products for particulate matter and discoloration prior to administration, whenever solution and container permit.
    • Administer THROMBATE III, once reconstituted, alone without mixing with other agents or diluents.
    • Administer within 3 hours following reconstitution. Do not refrigerate after reconstitution.
    • Adapt the rate of administration to the response of the individual patient, but administration of the entire dose in 10 to 20 minutes is generally well tolerated.
  • 3 DOSAGE FORMS AND STRENGTHS

    THROMBATE III is a sterile lyophilized powder for reconstitution in single use vials.  Each vial of THROMBATE III contains the labeled amount of antithrombin in units per vial, typically 500 units. When reconstituted with 10 mL of Sterile Water for Injection, USP, the final concentration is approximately 50 units per mL.

    The potency is determined with a standard calibrated in International Units against a World Health Organization (WHO) antithrombin reference preparation.

  • 4 CONTRAINDICATIONS

    None.

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Hypersensitivity Reactions

    Hypersensitivity reactions, including anaphylaxis, are possible. Early signs of hypersensitivity reactions, which can progress to anaphylaxis, may include angioedema, chest tightness, hypotension, rash, nausea, vomiting, paresthesia, restlessness, wheezing and dyspnea. If hypersensitivity symptoms occur, discontinue use of the product immediately and administer appropriate emergency treatment.

    5.2 Transmission of Infectious Agents

    Because THROMBATE III is made from human blood, it may carry a risk of transmitting infectious agents, e.g., viruses, the variant Creutzfeldt-Jakob disease (vCJD) agent and, theoretically, the Creutzfeldt-Jakob disease (CJD) agent. There is also the possibility that unknown infectious agents may be present in the product. The risk that the product will transmit viruses has been reduced by screening plasma donors for prior exposure to certain viruses, by testing for the presence of certain current virus infections, and by inactivating and removing certain viruses during manufacture. Despite these measures, this product may still potentially transmit diseases.     

    Report all infections suspected by a physician possibly to have been transmitted by this product to Grifols Therapeutics LLC at 1-800-520-2807.

    5.3 Monitoring: Laboratory Tests

    • The effect of drugs that use antithrombin to exert their anticoagulation may be altered when THROMBATE III is added or withdrawn. Regularly perform coagulation tests suitable for the anticoagulant used (e.g., aPTT and anti-Factor Xa activity) to avoid excessive or insufficient anticoagulation. Additionally, monitor the patients for the occurrence of bleeding or thrombosis. [see Drug Interactions (7)]
    • Measure functional levels of AT in plasma by amidolytic assays using chromogenic substrates or by clotting assays. Do not use immunoassays because they do not detect all hereditary AT deficiencies.
  • 6 ADVERSE REACTIONS

    In clinical studies, the most common adverse reactions (≥ 5% of subjects) were dizziness, chest discomfort, nausea, dysgeusia, and pain (cramps).

    6.1 Clinical Trials Experience

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

    Two clinical trials were conducted in 33 subjects with congenital AT deficiency. The first was a prospective, open-label, dose-escalation, dose-ranging, and pharmacokinetic study in 11 asymptomatic subjects. Eight subjects received a single dose, escalated sequentially, followed by weekly dose ranging from 25 to 125 unit/kg. Five subjects (including 2 from the first part of the study) received weekly THROMBATE III for periods of up to 23 weeks in doses ranging from 125 to 225 unit/kg. The second trial was a phase III, prospective, open-label study conducted in 24 subjects for additional kinetics (n=3), the prevention of thrombosis (n=13) during high risk conditions (pregnancy, surgery), or the treatment of thrombosis (n=10). Loading doses targeted an AT plasma level of 120% and ranged from 33 to 150 unit/kg. Maintenance doses targeted a plasma AT range of 70% to 120%, which were 23 to 75 unit/kg.

    Adverse reactions reported during the 2 clinical trials are listed in Table 2. Nine subjects (27%) experienced 29 adverse reactions which occurred during 17 of 389 infusions. There were no serious adverse reactions reported. The severity of adverse reactions was reported as mild or moderate, except for wound secretion and hematoma, which was severe.

    Table 2: Adverse Reactions Occurring during Hereditary Deficiency Trials
    *
    MedDRA Preferred Term; an adverse reaction is defined as any adverse event where either a) the event was related, or possibly related to the drug, b) the occurrence was during infusion or shortly after treatment,   or c) the event recurred after withdrawal and re-administration (challenge/dechallenge).
    N = 33 subjects
    N = 389 infusions
    Adverse Reaction*   Number of Subjects with
    Adverse Reaction (%) 
    Number of Adverse Reactions
    (% of All Infusions)
    Any adverse reaction 9 (27) 29 (7.5)
    Dizziness 4 (12) 8 (2.1)
    Chest discomfort 3 (9) 3 (0.8)
    Nausea 3 (9) 3 (0.8)
    Dysgeusia 2 (6) 3 (0.8)
    Pain (cramps) 2 (6) 2 (0.5)
    Chills 1 (3) 2 (0.5)
    Wound secretion and hematoma 1 (3) 2 (0.5)
    Vision blurred 1 (3) 1 (0.3)
    Chest pain 1 (3) 1 (0.3)
    Dyspnea 1 (3) 1 (0.3)
    Intestinal dilatation 1 (3) 1 (0.3)
    Pyrexia 1 (3) 1 (0.3)
    Urticaria 1 (3) 1 (0.3)

    During clinical investigation of THROMBATE III, there were no reports of virus transmission. None of 12 subjects monitored for a median of 8 months (range 2–19 months) after receiving THROMBATE III became antibody positive to human immunodeficiency virus (HIV-1). None of 14 subjects monitored for ≥ 3 months demonstrated any evidence of hepatitis.

  • 7 DRUG INTERACTIONS

    The anticoagulant effect of heparin is enhanced by concurrent treatment with THROMBATE III in patients with hereditary AT deficiency. Thus, in order to avoid bleeding, the dosage of heparin (or low molecular weight heparin) may need to be reduced during treatment with THROMBATE III.

    The effect of drugs that use antithrombin to exert their anticoagulation may be altered when THROMBATE III is added or withdrawn.  Regularly perform coagulation tests suitable for the anticoagulant used (e.g., aPTT and anti-Factor Xa activity) and at close intervals to avoid excessive or insufficient anticoagulation. Adjust dosage of anticoagulant as necessary. Additionally, monitor the patients for the occurrence of bleeding or thrombosis.

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    There are no data with THROMBATE III use in pregnant women to inform a drug-associated risk. However, there are clinical considerations [see Clinical Considerations]. It is not known whether THROMBATE III can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. THROMBATE III should be given to a pregnant woman only if clearly needed. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2-4% and 15-20%, respectively.

    Reproduction studies have been performed in rats and rabbits at doses up to four times the human dose and have revealed no evidence of impaired fertility or harm to the fetus due to THROMBATE III.

    Clinical Considerations

    Labor or Delivery

    Suspend heparin (or low molecular weight heparin) administration and continue THROMBATE III administration during labor and delivery.

    8.2 Lactation

    Risk Summary

    There is no information regarding the presence of THROMBATE III in human milk, the effects on the breastfed infant, or the effects on milk production. The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for THROMBATE III and any potential adverse effects on the breastfed infant from THROMBATE III or from the underlying maternal condition.

    8.4 Pediatric Use

    Safety and effectiveness in the pediatric population have not been established.

    8.5 Geriatric Use

    The safety and effectiveness in the geriatric population have not been established.

  • 11 DESCRIPTION

    THROMBATE III, Antithrombin III (Human), is a sterile, non-pyrogenic concentrate of human antithrombin (AT) in lyophilized powder form for reconstitution for intravenous injection. When reconstituted with Sterile Water for Injection, USP, THROMBATE III has a pH of 6.0 to 7.5 and contains 110 mEq/L to 210 mEq/L sodium, 110 mEq/L to 210 mEq/L chloride, 0.075 M to 0.125 M alanine, and not more than 0.1 unit of heparin per 1 unit of AT. THROMBATE III contains no preservative.

    THROMBATE III is prepared from pooled units of human plasma from normal donors. The capacity of the THROMBATE III manufacturing process to remove and/or inactivate enveloped and non-enveloped viruses has been validated by laboratory spiking studies on a scaled down process model using a wide range of viruses with diverse physicochemical properties. There are two dedicated virus inactivation/removal steps included in the THROMBATE III manufacturing process: a heat treatment step at 60°C ± 0.5°C for not less than 10 hours for virus inactivation and a nanofiltration step for effective removal of viruses as small as 18 nm.

    The THROMBATE III manufacturing process was also investigated for its capacity to decrease the infectivity of an experimental agent of transmissible spongiform encephalopathy (TSE), considered as a model for the variant Creutzfeldt-Jakob disease (vCJD) and Creutzfeldt-Jakob disease (CJD) agents. An individual production step in the THROMBATE III manufacturing process has been shown to decrease TSE infectivity of that experimental model agent. The TSE reduction step is the Effluent I to Effluent II + III fractionation step (6.0 log10). These studies provide reasonable assurance that low levels of vCJD/CJD agent infectivity, if present in the starting material, would be removed.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Antithrombin, an alpha2-glycoprotein of molecular weight 58,000, is normally present in human plasma at a concentration of approximately 12.5 mg/dL and is the major plasma inhibitor of thrombin. Inactivation of thrombin by AT occurs by formation of a covalent bond resulting in an inactive 1:1 stoichiometric complex between the two, involving an interaction of the active serine of thrombin and an arginine reactive site on AT. AT is also capable of inactivating other components of the coagulation cascade including factors IXa, Xa, XIa, and XIIa, as well as plasmin. The neutralization rate of serine proteases by AT proceeds slowly in the absence of heparin, but is greatly accelerated in the presence of heparin. As the therapeutic antithrombotic effect of heparin is mediated by AT, heparin in vivo is ineffective in the absence or near absence of AT.

    After administration, THROMBATE III temporarily replaces the missing AT in patients with hereditary antithrombin deficiency.

    12.3 Pharmacokinetics

    In a clinical trial of THROMBATE III conducted in asymptomatic subjects with hereditary deficiency of AT, 8 subjects were administered a single dose of THROMBATE III at doses ranging from 25 units/kg to 125 units/kg. Pharmacokinetic parameters were determined using immunologic and functional AT assays (Table 3).

    Table 3: Pharmacokinetic Analyses of THROMBATE III in Asymptomatic Subjects with Congenital AT Deficiency
      Immunological Assay Functional Assay
    *
    Mean ± SEM
    AT recovery, % / unit / kg 1.6 ± 0.1* 1.4 ± 0.1
    50% disappearance time, hr 17.4 ± 3.9 22.3 ± 8.6
    t½, day 2.5 ± 1.5 3.8 ± 1.8
  • 14 CLINICAL STUDIES

    In a prospective, open-label clinical trial, 21 subjects were administered THROMBATE III for 16 prophylaxis events (n=13 subjects) and 10 for treatment of thrombosis (n=10 subjects) with 2 subjects receiving THROMBATE III for both prophylaxis and treatment of thrombosis. None of the 13 subjects with hereditary AT deficiency and histories of thromboembolism treated prophylactically on 16 separate occasions with THROMBATE III for high thrombotic risk situations (11 surgical procedures, 5 pregnancies and/or deliveries) developed a thrombotic complication. Heparin was administered in 3 of the 11 surgical procedures. Two of the pregnant subjects received LMW heparin prophylactically during the first trimester, but which was unable to maintain anti-coagulation with increasing dosages. [see Drug Interactions (7)] They experienced a thrombosis, which subsequently resolved with the addition of THROMBATE III, and were therefore administered THROMBATE III and LMW heparin prophylaxis weekly during the second and third trimesters, and during labor and delivery. These two subjects did not experience a new thrombosis.

    Ten subjects with hereditary AT deficiency were treated with THROMBATE III as well as heparin (n=9) for major thrombotic or thromboembolic complications, including 4 subjects with thrombosis during the first trimester of pregnancy.  Nine subjects recovered with no additional thromboses or extension of existing thrombosis. The tenth subject died due to complications from the original pulmonary embolism with infarction which preceded treatment with THROMBATE III.

  • 15 REFERENCES

    1. Schwartz RS, Bauer KA, Rosenberg RD, et al. Clinical experience with antithrombin III concentrate in treatment of congenital and acquired deficiency of antithrombin. Am J Med. 1989;87 (Suppl 3B):53S-60S.
    2. Mannucci PM, Boyer C, Wolf M, et al. Treatment of congenital antithrombin III deficiency with concentrates. Br J Haematol. 1982;50(3):531-5.
    3. Collen D, Schetz J, de Cock F, et al. Metabolism of antithrombin III (heparin cofactor) in man: effects of venous thrombosis and of heparin administration. Eur J Clin Invest. 1977;7(1):27-35.
    4. Marciniak E, Gockerman JP. Heparin-induced decrease in circulating antithrombin-III. Lancet. 1977;2(8038):581-4.
    5. O’Brien JR, Etherington MD. Effect of heparin and warfarin on antithrombin III. Lancet. 1977;2(8050):1232.
    6. Kakkar VV, Bentley PG, Scully MF, et al. Antithrombin III and heparin. Lancet. 1980;1(8159):103-4.
  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    THROMBATE III is supplied in a kit containing one single use vial of THROMBATE III lyophilized powder for reconstitution, one vial of Sterile Water for Injection, USP, one sterile double-ended transfer needle, and one sterile filter needle. The total activity of AT in International Units is stated on the label of the THROMBATE III vial.

     Components of the packaging do not contain natural rubber latex.

    NDC Number
    Carton (Kit)
    Approximate
    Antithrombin Potency
    Diluent
    13533-603-20
    or
    13533-602-50
    500 units 10 mL
    • Store THROMBATE III at temperatures not to exceed 25°C (77°F).
    • Avoid freezing as breakage of the diluent vial might occur.
  • 17 PATIENT COUNSELING INFORMATION

    Hypersensitivity Reactions

    Inform patients that allergic-type hypersensitivity reactions are possible and instruct them to inform their physicians about any past or present known hypersensitivity to human plasma proteins prior to treatment with THROMBATE III. Inform patients of the early signs of hypersensitivity reactions including hives, generalized urticaria, tightness of the chest, wheezing, hypotension, and anaphylaxis and to notify their health care provider immediately if these events develop. [see Warnings and Precautions (5.1)]

    Transmission of Infectious Disease

    Inform patients that THROMBATE III is made from human plasma and may carry a risk of transmitting infectious agents that can cause disease (e.g., viruses, the variant Creutzfeldt-Jakob disease (vCJD) agent and, theoretically, the Creutzfeldt-Jakob disease (CJD) agent). Inform patients that this risk has been reduced by screening plasma donors for prior exposure to certain infectious agents, by testing the donated plasma for markers of certain current infections, and by inactivating and/or removing pathogens during manufacturing. [see Warnings and Precautions (5.2)]

    Manufactured by:

    GRIFOLS

    Grifols Therapeutics LLC
    Research Triangle Park, NC 27709 USA
    U.S. License No. 1871

    3052613

  • PACKAGE LABEL

    NDC 13533-605-21

    Antithrombin III (Human)

    THROMBATE III®

    Heat-Treated

    Nanofiltered

    Lyophilized Powder

    For Intravenous Administration Only

    Grifols Therapeutics LLC
    Research Triangle Park, NC 27709 USA
    U.S. License No. 1871

    The patient and physician should discuss the risks and benefits of this product.

    No Preservative
    Sterile — Nonpyrogenic

    Reconstitute with 10 mL Sterile Water for Injection, USP.

    Store at temperatures not to exceed 25°C (77°F). Do not freeze.

    Dosage and Administration: Read package insert.

    Rx only

    3051796

    Lot

    Exp.

    IU

    Thrombate III Vial

    NDC 13533-602-50

    Antithrombin III (Human)

    THROMBATE III®

    Heat-Treated

    Nanofiltered

    Lyophilized Powder

    For Intravenous Administration Only

    Grifols

    CONTENTS:
    One bottle of THROMBATE III
    10 mL Sterile Water for Injection, USP
    One sterile filter needle
    One sterile double-ended transfer needle

    No Preservative
    Sterile—Nonpyrogenic

    THIS PRODUCT IS PREPARED FROM LARGE POOLS OF HUMAN PLASMA WHICH MAY CONTAIN INFECTIOUS AGENTS. SEE PACKAGE INSERT WARNINGS.


    The patient and physician should discuss the risks and benefits of this product.

    The product when reconstituted with 10 mL Sterile Water for Injection, USP, contains 110–210 mEq/L sodium, 110 –210 mEq/L chloride, 0.075–0.125 M alanine, and not more than 0.1 IU heparin/IU ATIII.

    Administer within 3 hours after reconstitution.

    Dosage and Administration: Read enclosed package insert.

    Store at temperatures not to exceed 25°C (77°F). Do not freeze.

    If the shrink band is absent or shows any sign of tampering, do not use the product and notify Grifols Therapeutics LLC immediately.

    Not Returnable for Credit or Exchange

    Rx only

    CAUTION: U.S. federal law prohibits dispensing without prescription.

    Grifols Therapeutics LLC
    Research Triangle Park,
    NC 27709 USA
    U.S. License No. 1871

    Open other end

    Carton: 3046696

    GTIN XXXXXXXXXXXXXX
    LOT   XXXXXXXXXX
    EXP   DDMMMYYYY
    IU      XXX
    SN     XXXXXXXXXXXXXXXX

    Thrombate III Carton

    NDC 13533-200-10

    Sterile Water for Injection, USP

    10 mL

    Rx Only

    For reconstitution of accompanying product

    Single-Dose Container, Nonpyrogenic

    Do not use unless clear.

    No antimicrobial agent or other substance has been added.

    Do not use for intravascular injection without making approximately isotonic by addition of suitable solute.

    Discard unused portion.

    Mfd by: Laboratorios Grifols, S. A., Parets del Vallès, Barcelona, 08150 Spain
    Mfd for: Grifols Therapeutics LLC, Research Triangle Park, NC, 27709 USA

    3051810

    Lot / Exp.

    Thrombate III Diluent
  • INGREDIENTS AND APPEARANCE
    THROMBATE III  
    antithrombin iii (human) kit
    Product Information
    Product TypePLASMA DERIVATIVEItem Code (Source)NDC:13533-603
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13533-603-201 in 1 CARTON; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 VIAL, GLASS 10 mL
    Part 21 VIAL, GLASS 10 mL
    Part 1 of 2
    THROMBATE III  
    antithrombin iii (human) injection, powder, lyophilized, for solution
    Product Information
    Item Code (Source)NDC:13533-605
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Antithrombin Iii Human (UNII: T0LTO7L82X) (Antithrombin Iii Human - UNII:T0LTO7L82X) Antithrombin Iii Human50 [iU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Alanine (UNII: OF5P57N2ZX)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13533-605-2110 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10319612/30/1991
    Part 2 of 2
    STERILE WATER  
    water injection
    Product Information
    Item Code (Source)NDC:13533-000
    Route of AdministrationINTRAVENOUS
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13533-000-0510 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10319612/30/1991
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10319612/30/1991
    THROMBATE III  
    antithrombin iii (human) kit
    Product Information
    Product TypePLASMA DERIVATIVEItem Code (Source)NDC:13533-604
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13533-604-251 in 1 CARTON; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 VIAL, GLASS 10 mL
    Part 21 VIAL, GLASS 10 mL
    Part 1 of 2
    THROMBATE III  
    antithrombin iii (human) injection, powder, lyophilized, for solution
    Product Information
    Item Code (Source)NDC:13533-605
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Antithrombin Iii Human (UNII: T0LTO7L82X) (Antithrombin Iii Human - UNII:T0LTO7L82X) Antithrombin Iii Human50 [iU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Alanine (UNII: OF5P57N2ZX)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13533-605-2110 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10319612/30/1991
    Part 2 of 2
    STERILE WATER  
    water injection
    Product Information
    Item Code (Source)NDC:13533-100
    Route of AdministrationINTRAVENOUS
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13533-100-5010 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10319612/30/1991
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10319612/30/199106/22/2017
    THROMBATE III  
    antithrombin iii (human) kit
    Product Information
    Product TypePLASMA DERIVATIVEItem Code (Source)NDC:13533-602
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13533-602-501 in 1 CARTON; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 VIAL, GLASS 10 mL
    Part 21 VIAL, GLASS 10 mL
    Part 1 of 2
    THROMBATE III  
    antithrombin iii (human) injection, powder, lyophilized, for solution
    Product Information
    Item Code (Source)NDC:13533-605
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Antithrombin Iii Human (UNII: T0LTO7L82X) (Antithrombin Iii Human - UNII:T0LTO7L82X) Antithrombin Iii Human50 [iU]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Alanine (UNII: OF5P57N2ZX)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13533-605-2110 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10319612/30/1991
    Part 2 of 2
    STERILE WATER  
    water injection
    Product Information
    Item Code (Source)NDC:13533-200
    Route of AdministrationINTRAVENOUS
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13533-200-1010 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10319612/30/1991
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA10319612/30/1991
    Labeler - GRIFOLS USA, LLC (048987452)
    Establishment
    NameAddressID/FEIBusiness Operations
    GRIFOLS THERAPEUTICS LLC611019113manufacture(13533-602, 13533-603, 13533-604, 13533-605)