Label: CEFTRIAXONE- ceftriaxone sodium injection, powder, for solution

  • NDC Code(s): 0143-9856-01, 0143-9856-25, 0143-9857-01, 0143-9857-25, view more
    0143-9858-01, 0143-9858-25, 0143-9859-01, 0143-9859-25
  • Packager: West-Ward Pharmaceutical Corp
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated 07/14

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  • SPL UNCLASSIFIED SECTION

    Rx Only

    To reduce the development of drug-resistant bacteria and maintain the effectiveness of ceftriaxone for injection and other antibacterial drugs, ceftriaxone for injection should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.

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  • DESCRIPTION

    Ceftriaxone for Injection, USP is a sterile, semisynthetic, broad-spectrum cephalosporin antibiotic for intravenous or intramuscular administration. Ceftriaxone sodium is (6R,7R)-7-[2-(2-Amino-4-thiazolyl)glyoxylamido]-8-oxo-3-[[(1,2,5,6-tetrahydro-2-methyl-5,6-dioxo-as-triazin-3-yl)thio]methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 72-(Z)-(O-methyloxime), disodium salt, sesquaterhydrate.

    The chemical formula of ceftriaxone sodium is C18H16N8Na2O7S3•3.5H2O. It has a calculated molecular weight of 661.59 and the following structural formula:

    Structural formula

    Ceftriaxone for Injection, USP is a white to yellowish-orange crystalline powder which is readily soluble in water, sparingly soluble in methanol and very slightly soluble in ethanol. The pH of a 1% aqueous solution is approximately 6.7. The color of Ceftriaxone for Injection, USP solutions ranges from light yellow to amber, depending on the length of storage, concentration and diluent used.

    Ceftriaxone for Injection, USP contains approximately 83 mg (3.6 mEq) of sodium per gram of ceftriaxone activity.

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  • CLINICAL PHARMACOLOGY

    Average plasma concentrations of ceftriaxone following a single 30 minute intravenous (IV) infusion of a 0.5, 1 or 2 gm dose and intramuscular (IM) administration of a single 0.5 (250 mg/mL or 350 mg/mL concentrations) or 1 gm dose in healthy subjects are presented in Table 1.

    TABLE 1. Ceftriaxone Plasma Concentrations After Single Dose Administration
      Dose/Route   Average Plasma Concentrations (mcg/mL)
          0.5 hr  1 hr  2 hr   4 hr   6 hr   8 hr   12 hr   16 hr   24 hr
      0.5 gm IV* 82  59 48 37  29 23 15 10 5
      0.5 gm IM
       250 mg/mL
    22  33  38  35   30 26 16 ND 5
      0.5 gm IM
       350 mg/mL
    20  32  38  34   31 24 16 ND 5
      1 gm IV* 151   111  88  67   53 43 28 18 9
      1 gm IM 40  68  76  68   56 44  29 ND ND
      2 gm IV* 257   192   154   117   89 74 46 31 15
    ND = Not determined.
    * IV doses were infused at a constant rate over 30 minutes.

    Ceftriaxone was completely absorbed following IM administration with mean maximum plasma concentrations occurring between 2 and 3 hours post-dose. Multiple IV or IM doses ranging from 0.5 to 2 gm at 12 to 24 hour intervals resulted in 15% to 36% accumulation of ceftriaxone above single dose values.

    Ceftriaxone concentrations in urine are shown in Table 2.

    TABLE 2. Urinary Concentrations of Ceftriaxone After Single Dose Administration
      Dose/Route   Average Urinary Concentrations (mcg/mL)
          0 - 2 hr   2 - 4 hr   4 - 8 hr   8 - 12 hr   12 - 24 hr   24 - 48 hr
      0.5 gm IV   526   366   142   87   70   15
      0.5 gm IM   115   425   308   127   96   28
      1 gm IV   995   855   293   147   132   32
      1 gm IM   504   628   418   237   ND   ND
      2 gm IV   2692   1976   757   274   198   40
      ND = Not determined.

    Thirty-three percent to 67% of a ceftriaxone dose was excreted in the urine as unchanged drug and the remainder was secreted in the bile and ultimately found in the feces as microbiologically inactive compounds. After a 1 gm IV dose, average concentrations of ceftriaxone, determined from 1 to 3 hours after dosing, were 581 mcg/mL in the gallbladder bile, 788 mcg/mL in the common duct bile, 898 mcg/mL in the cystic duct bile, 78.2 mcg/gm in the gallbladder wall and 62.1 mcg/mL in the concurrent plasma.

    Over a 0.15 to 3 gm dose range in healthy adult subjects, the values of elimination half-life ranged from 5.8 to 8.7 hours; apparent volume of distribution from 5.78 to 13.5 L; plasma clearance from 0.58 to 1.45 L/hour; and renal clearance from 0.32 to 0.73 L/hour.

    Ceftriaxone is reversibly bound to human plasma proteins, and the binding decreased from a value of 95% bound at plasma concentrations of < 25 mcg/mL to a value of 85% bound at 300 mcg/mL. Ceftriaxone crosses the blood placenta barrier.

    The average values of maximum plasma concentration, elimination half-life, plasma clearance and volume of distribution after a 50 mg/kg IV dose and after a 75 mg/kg IV dose in pediatric patients suffering from bacterial meningitis are shown in Table 3.

    Ceftriaxone penetrated the inflamed meninges of infants and pediatric patients; CSF concentrations after a 50 mg/kg IV dose and after a 75 mg/kg IV dose are also shown in Table 3.

    TABLE 3. Average Pharmacokinetic Parameters of Ceftriaxone in Pediatric Patients With Meningitis
        50 mg/kg IV 75 mg/kg IV
     Maximum Plasma Concentrations (mcg/mL) 216 275
     Elimination Half-life (hr) 4.6 4.3
     Plasma Clearance (mL/hr/kg) 49 60
     Volume of Distribution (mL/kg) 338 373
     CSF Concentration - inflamed meninges (mcg/mL) 5.6 6.4
     Range (mcg/mL) 1.3 - 18.5 1.3 - 44
     Time after dose (hr) 3.7 (± 1.6) 3.3 (± 1.4)

    Compared to that in healthy adult subjects, the pharmacokinetics of ceftriaxone were only minimally altered in elderly subjects and in patients with renal impairment or hepatic dysfunction (Table 4); therefore, dosage adjustments are not necessary for these patients with ceftriaxone dosages up to 2 gm per day. Ceftriaxone was not removed to any significant extent from the plasma by hemodialysis; in six of 26 dialysis patients, the elimination rate of ceftriaxone was markedly reduced.

    TABLE 4. Average Pharmacokinetic Parameters of Ceftriaxone in Humans
    Subject Group Elimination Half-Life
    (hr)
    Plasma Clearance
    (L/hr)
    Volume of Distribution
    (L)
     Healthy Subjects 5.8 - 8.7 0.58 - 1.45 5.8 - 13.5
     Elderly Subjects (mean age, 70.5 yr) 8.9 0.83 10.7
     Patients With Renal Impairment         
     Hemodialysis Patients (0 - 5 mL/min)*  14.7 0.65 13.7
     Severe (5 - 15 mL/min) 15.7 0.56 12.5
     Moderate (16 - 30 mL/min) 11.4 0.72 11.8
     Mild (31 - 60 mL/min) 12.4 0.70 13.3
     Patients With Liver Disease 8.8 1.1 13.6

    *Creatinine clearance.

    The elimination of ceftriaxone is not altered when ceftriaxone for injection is co-administered with probenecid.

    Pharmacokinetics in the Middle Ear Fluid

    In one study, total ceftriaxone concentrations (bound and unbound) were measured in middle ear fluid obtained during the insertion of tympanostomy tubes in 42 pediatric patients with otitis media. Sampling times were from 1 to 50 hours after a single intramuscular injection of 50 mg/kg of ceftriaxone. Mean (± SD) ceftriaxone levels in the middle ear reached a peak of 35 (± 12) mcg/mL at 24 hours, and remained at 19 (± 7) mcg/‌mL at 48 hours. Based on middle ear fluid ceftriaxone concentrations in the 23 to 25 hour and the 46 to 50 hour sampling time intervals, a half-life of 25 hours was calculated. Ceftriaxone is highly bound to plasma proteins. The extent of binding to proteins in the middle ear fluid is unknown.

    Interaction with Calcium

    Two in vitro studies, one using adult plasma and the other neonatal plasma from umbilical cord blood have been carried out to assess interaction of ceftriaxone and calcium. Ceftriaxone concentrations up to 1 mM (in excess of concentrations achieved in vivo following administration of 2 grams ceftriaxone infused over 30 minutes) were used in combination with calcium concentrations up to 12 mM (48 mg/‌dL). Recovery of ceftriaxone from plasma was reduced with calcium concentrations of 6 mM (24 mg/‌dL) or higher in adult plasma or 4 mM (16 mg/‌dL) or higher in neonatal plasma. This may be reflective of ceftriaxone-calcium precipitation.

    Microbiology

    Mechanism of Action

    Ceftriaxone is a bactericidal agent that acts by inhibition of bacterial cell wall synthesis. Ceftriaxone has activity in the presence of some beta-lactamases, both penicillinases and cephalosporinases, of Gram-negative and Gram-positive bacteria.

    Mechanism of Resistance

    Resistance to ceftriaxone is primarily through hydrolysis by beta-lactamase, alteration of penicillin-binding proteins (PBPs), and decreased permeability.

    Interaction with Other Antimicrobials

    In an in vitro study antagonistic effects have been observed with the combination of chloramphenicol and ceftriaxone.

    Ceftriaxone has been shown to be active against most isolates of the following bacteria, both in vitro and in clinical infections described in the INDICATIONS AND USAGE section:

    Gram-negative bacteria
    Acinetobacter calcoaceticus
    Enterobacter aerogenes
    Enterobacter cloacae
    Escherichia coli
    Haemophilus influenzae
    Haemophilus parainfluenzae
    Klebsiella oxytoca
    Klebsiella pneumoniae
    Moraxella catarrhalis
    Morganella morganii
    Neisseria gonorrhoeae
    Neisseria meningitidis
    Proteus mirabilis
    Proteus vulgaris
    Pseudomonas aeruginosa
    Serratia marcescens

    Gram-positive bacteria
    Staphylococcus aureus
    Staphylococcus epidermidis
    Streptococcus pneumoniae
    Streptococcus pyogenes
    Viridans group streptococci

    Anaerobic bacteria
    Bacteroides fragilis
    Clostridium species
    Peptostreptococcus species

    The following in vitro data are available, but their clinical significance is unknown. At least 90 percent of the following microorganisms exhibit an in vitro minimum inhibitory concentration (MIC) less than or equal to the susceptible breakpoint for ceftriaxone. However, the efficacy of ceftriaxone in treating clinical infections due to these microorganisms has not been established in adequate and well-controlled clinical trials.

    Gram-negative bacteria
    Citrobacter diversus
    Citrobacter freundii
    Providencia species (including Providencia rettgeri)
    Salmonella species (including Salmonella typhi)
    Shigella species

    Gram-positive bacteria
    Streptococcus agalactiae

    Anaerobic bacteria
    Porphyromonas (Bacteroides) melaninogenicus
    Prevotella (Bacteroides) bivius

    Susceptibility Test Methods

    When available, the clinical microbiology laboratory should provide the results of in vitro susceptibility test results for antimicrobial drug products used in resident hospitals to the physician as periodic reports that describe the susceptibility profile of nosocomial and community-acquired pathogens. These reports should aid the physician in selecting an antibacterial drug product for treatment.

    Dilution Techniques:

    Quantitative methods are used to determine antimicrobial minimal inhibitory concentrations (MICs). These MICs provide estimates of the susceptibility of bacteria to antimicrobial compounds. The MICs should be determined using a standardized test method.1,3  The MIC values should be interpreted according to criteria provided in Table 6.

    Diffusion Techniques:

    Quantitative methods that require measurement of zone diameters also provide reproducible estimates of the susceptibility of bacteria to antimicrobial compounds. The zone size provides an estimate of the susceptibility of bacteria to antimicrobial compounds. The zone size should be determined using a standardized test method.2,3 This procedure uses paper disks impregnated with 30 mcg ceftriaxone to test the susceptibility of microorganisms to ceftriaxone. The disk diffusion interpretive criteria are provided in Table 6.

    Anaerobic techniques:

    For anaerobic bacteria, the susceptibility to ceftriaxone as MICs can be determined by a standardized agar test method.3,4  The MIC values obtained should be interpreted according to the criteria provided in Table 6:


    Table 6. Susceptibility Test Interpretive Criteria for Ceftriaxone

    Pathogen

    Minimum Inhibitory Concentrations
    (mcg/ml)

    Disk Diffusion Zone Diameters
    (mm)

    (S) Susceptible

    (I) Intermediate

    (R) Resistant

    (S) Susceptible

    (I) Intermediate

    (R) Resistant

    Enterobacteriaceae

    ≤ 1

    2

    ≥ 4

    ≥ 23

    20 - 22

    ≤ 19

    Haemophilus influenzae*

    ≤ 2

    -

    -

    ≥ 26

    -

    -

    Neisseria gonorrhoeae*

    ≤ 0.25

    -

    -

    ≥ 35

    -

    -

    Neisseria meningitidis*

    ≤ 0.12

    -

    -

    ≥ 34

    -

    -

    Streptococcus pneumoniae meningitis isolates

    ≤ 0.5

    1

    ≥ 2

    -

    -

    -

    Streptococcus pneumoniae non-meningitis isolates

    ≤ 1

    2

    ≥ 4

    -

    -

    -

    Streptococcus species beta-hemolytic group*

    ≤ 0.5

    -

    -

    ≥ 24

    -

    -

    Viridans group streptococci

    ≤ 1

    2

    ≥ 4

    ≥ 27

    25 - 26

    ≤ 24

    Anaerobic bacteria (agar method)

    ≤ 16

    32

    ≥ 64

    -

    -

    -

    Susceptibility of staphylococci to ceftriaxone may be deduced from testing only penicillin and either cefoxitin or oxacillin.

    * ​​The current absence of data on resistant isolates precludes defining any category other than 'Susceptible'. If isolates yield MIC results other than susceptible, they should be submitted to a reference laboratory for additional testing.

    Disc diffusion interpretive criteria for ceftriaxone discs against Streptococcus pneumoniae are not available, however, isolates of pneumococci with oxacillin zone diameters of >20 mm are susceptible (MIC ≤ 0.06 mcg/mL) to penicillin and can be considered susceptible to ceftriaxone. Streptococcus pneumoniae isolates should not be reported as penicillin (ceftriaxone) resistant or intermediate based solely on an oxacillin zone diameter of ≤ 19 mm. The ceftriaxone MIC should be determined for those isolates with oxacillin zone diameters ≤ 19 mm.

    A report of Susceptible indicates that the antimicrobial is likely to inhibit growth of the pathogen if the antimicrobial compound reaches the concentration at the infection site necessary to inhibit growth of the pathogen. A report of Intermediate indicates that the result should be considered equivocal, and if the microorganism is not fully susceptible to alternative, clinically feasible drugs, the test should be repeated. This category implies possible clinical applicability in body sites where the drug is physiologically concentrated or in situations where a high dosage of drug can be used. This category also provides a buffer zone that prevents small uncontrolled technical factors from causing major discrepancies in interpretation. A report of Resistant indicates that the antimicrobial is not likely to inhibit growth of the pathogen if the antimicrobial compound reaches the concentrations usually achievable at the infection site; other therapy should be selected.

    Quality Control:

    Standardized susceptibility test procedures require the use of laboratory controls to monitor and ensure the accuracy and precision of supplies and reagents used in the assay, and the techniques of the individual performing the test.1,2,3,4  Standard ceftriaxone powder should provide the following range of MIC values noted in Table 7. For the diffusion technique using the 30 mcg disk, the criteria in Table 7 should be achieved.

    Table 7. Acceptable Quality Control Ranges for Ceftriaxone

    QC Strain

    Minimum Inhibitory Concentrations
    (mcg/mL)

    Disk Diffusion Zone diameters
    (mm)

    Escherichia coli ATCC 25922

    0.03 - 0.12

    29 - 35

    Staphylococcus aureus ATCC 25923

    ----------

    22 - 28

    Staphylococcus aureus ATCC 29213

    1 - 8

    ---------

    Haemophilus influenzae ATCC 49247

    0.06 - 0.25

    31 - 39

    Neisseria gonorrhoeae ATCC 49226

    0.004 - 0.015

    39 - 51

    Pseudomonas aeruginosa ATCC 27853

    8 - 64

    17 - 23

    Streptococcus pneumoniae ATCC 49619

    0.03 - 0.12

    30 - 35

    Bacteroides fragilis ATCC 25285 (agar method)

    32 - 128

    ---------

    Bacteroides thetaiotaomicron ATCC 29741 (agar method)

    64 - 256

    ---------

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  • INDICATIONS AND USAGE

    Before instituting treatment with Ceftriaxone for Injection, USP, appropriate specimens should be obtained for isolation of the causative organism and for determination of its susceptibility to the drug. Therapy may be instituted prior to obtaining results of susceptibility testing.

    To reduce the development of drug-resistant bacteria and maintain the effectiveness of Ceftriaxone for Injection, USP and other antibacterial drugs, Ceftriaxone for Injection, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.

    Ceftriaxone for Injection, USP is indicated for the treatment of the following infections when caused by susceptible organisms:

    LOWER RESPIRATORY TRACT INFECTIONS caused by Streptococcus pneumoniae, Staphylococcus aureus, Haemophilus influenzae, Haemophilus parainfluenzae, Klebsiella pneumoniae, Escherichia coli, Enterobacter aerogenes, Proteus mirabilis or Serratia marcescens.

    ACUTE BACTERIAL OTITIS MEDIA caused by Streptococcus pneumoniae, Haemophilus influenzae (including beta‑lactamase producing strains) or Moraxella catarrhalis (including beta-lactamase producing strains).

    NOTE: In one study lower clinical cure rates were observed with a single dose of Ceftriaxone for Injection, USP compared to 10 days of oral therapy. In a second study comparable cure rates were observed between single dose of Ceftriaxone for Injection, USP and the comparator. The potentially lower clinical cure rate of Ceftriaxone for Injection, USP should be balanced against the potential advantages of parenteral therapy (see CLINICAL STUDIES).

    SKIN AND SKIN STRUCTURE INFECTIONS caused by Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pyogenes, Viridans group streptococci, Escherichia coli, Enterobacter cloacae, Klebsiella oxytoca, Klebsiella pneumoniae, Proteus mirabilis, Morganella morganii1, Pseudomonas aeruginosa, Serratia marcescens, Acinetobacter calcoaceticus, Bacteroides fragilis1 or Peptostreptococcus species.

    URINARY TRACT INFECTIONS (complicated and uncomplicated) caused by Escherichia coli, Proteus mirabilis, Proteus vulgaris, Morganella morganii or Klebsiella pneumoniae.

    UNCOMPLICATED GONORRHEA (cervical/urethral and rectal) caused by Neisseria gonorrhoeae, including both penicillinase- and nonpenicillinase-producing strains, and pharyngeal gonorrhea caused by nonpenicillinase‑producing strains of Neisseria gonorrhoeae.

    PELVIC INFLAMMATORY DISEASE caused by Neisseria gonorrhoeae. Ceftriaxone for Injection, USP, like other cephalosporins, has no activity against Chlamydia trachomatis. Therefore, when cephalosporins are used in the treatment of patients with pelvic inflammatory disease and Chlamydia trachomatis is one of the suspected pathogens, appropriate antichlamydial coverage should be added.

    BACTERIAL SEPTICEMIA caused by Staphylococcus aureus, Streptococcus pneumoniae, Escherichia coli, Haemophilus influenzae or Klebsiella pneumoniae.

    BONE AND JOINT INFECTIONS caused by Staphylococcus aureus, Streptococcus pneumoniae, Escherichia coli, Proteus mirabilis, Klebsiella pneumoniae or Enterobacter species.

    INTRA-ABDOMINAL INFECTIONS caused by Escherichia coli, Klebsiella pneumoniae, Bacteroides fragilis, Clostridium species (Note: most strains of Clostridium difficile are resistant) or Peptostreptococcus species.

    MENINGITIS caused by Haemophilus influenzae, Neisseria meningitidis or Streptococcus pneumoniae. Ceftriaxone for Injection, USP has also been used successfully in a limited number of cases of meningitis and shunt infection caused by Staphylococcus epidermidis1 and Escherichia coli.1

    1Efficacy for this organism in this organ system was studied in fewer than ten infections.

    SURGICAL PROPHYLAXIS

    The preoperative administration of a single 1 gm dose of Ceftriaxone for Injection, USP may reduce the incidence of postoperative infections in patients undergoing surgical procedures classified as contaminated or potentially contaminated (e.g., vaginal or abdominal hysterectomy or cholecystectomy for chronic calculous cholecystitis in high-risk patients, such as those over 70 years of age, with acute cholecystitis not requiring therapeutic antimicrobials, obstructive jaundice or common duct bile stones) and in surgical patients for whom infection at the operative site would present serious risk (e.g., during coronary artery bypass surgery). Although Ceftriaxone for Injection, USP has been shown to have been as effective as cefazolin in the prevention of infection following coronary artery bypass surgery, no placebo-controlled trials have been conducted to evaluate any cephalosporin antibiotic in the prevention of infection following coronary artery bypass surgery.

    When administered prior to surgical procedures for which it is indicated, a single 1 gm dose of Ceftriaxone for Injection, USP provides protection from most infections due to susceptible organisms throughout the course of the procedure.

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  • CONTRAINDICATIONS

    Ceftriaxone is contraindicated in patients with known allergy to the cephalosporin class of antibiotics.

    Neonates (28 days)

    Hyperbilirubinemic neonates, especially prematures, should not be treated with ceftriaxone. In vitro studies have shown that ceftriaxone can displace bilirubin from its binding to serum albumin, leading to a possible risk of bilirubin encephalopathy in these patients.

    Ceftriaxone is contraindicated in neonates if they require (or are expected to require) treatment with calcium‑containing IV solutions, including continuous calcium-containing infusions such as parenteral nutrition because of the risk of precipitation of ceftriaxone-calcium (see CLINICAL PHARMACOLOGYWARNINGS and DOSAGE AND ADMINISTRATION).

    A small number of cases of fatal outcomes in which a crystalline material was observed in the lungs and kidneys at autopsy have been reported in neonates receiving ceftriaxone and calcium-containing fluids. In some of these cases, the same intravenous infusion line was used for both ceftriaxone and calcium-containing fluids and in some a precipitate was observed in the intravenous infusion line. At least one fatality has been reported in a neonate in whom ceftriaxone and calcium-containing fluids were administered at different time points via different intravenous lines; no crystalline material was observed at autopsy in this neonate. There have been no similar reports in patients other than neonates.

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  • WARNINGS

    Hypersensitivity

    BEFORE THERAPY WITH CEFTRIAXONE IS INSTITUTED, CAREFUL INQUIRY SHOULD BE MADE TO DETERMINE WHETHER THE PATIENT HAS HAD PREVIOUS HYPERSENSITIVITY REACTIONS TO CEPHALOSPORINS, PENICILLINS OR OTHER DRUGS. THIS PRODUCT SHOULD BE GIVEN CAUTIOUSLY TO PENICILLIN‑SENSITIVE PATIENTS. ANTIBIOTICS SHOULD BE ADMINISTERED WITH CAUTION TO ANY PATIENT WHO HAS DEMONSTRATED SOME FORM OF ALLERGY, PARTICULARLY TO DRUGS. SERIOUS ACUTE HYPERSENSITIVITY REACTIONS MAY REQUIRE THE USE OF SUBCUTANEOUS EPINEPHRINE AND OTHER EMERGENCY MEASURES.

    As with other cephalosporins, anaphylactic reactions with fatal outcome have been reported, even if a patient is not known to be allergic or previously exposed.

    Interaction with Calcium-Containing Products

    Do not use diluents containing calcium, such as Ringer’s solution or Hartmann’s solution, to reconstitute ceftriaxone vials or to further dilute a reconstituted vial for IV administration because a precipitate can form. Precipitation of ceftriaxone-calcium can also occur when ceftriaxone is mixed with calcium-containing solutions in the same IV administration line. Ceftriaxone must not be administered simultaneously with calcium-containing IV solutions, including continuous calcium-containing infusions such as parenteral nutrition via a Y-site. However, in patients other than neonates, ceftriaxone and calcium-containing solutions may be administered sequentially of one another if the infusion lines are thoroughly flushed between infusions with a compatible fluid. In vitro studies using adult and neonatal plasma from umbilical cord blood demonstrated that neonates have an increased risk of precipitation of ceftriaxone-calcium (see CLINICAL PHARMACOLOGYCONTRAINDICATIONS and DOSAGE AND ADMINISTRATION).

    Clostridium difficile

    Clostridium difficile associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including ceftriaxone, and may range in severity from mild diarrhea to fatal colitis. Treatment with antibacterial agents alters the normal flora of the colon leading to overgrowth of C. difficile.

    C. difficile produces toxins A and B which contribute to the development of CDAD. Hypertoxin producing strains of C. difficile cause increased morbidity and mortality, as these infections can be refractory to antimicrobial therapy and may require colectomy. CDAD must be considered in all patients who present with diarrhea following antibiotic use. Careful medical history is necessary since CDAD has been reported to occur over two months after the administration of antibacterial agents.

    If CDAD is suspected or confirmed, ongoing antibiotic use not directed against C. difficile may need to be discontinued. Appropriate fluid and electrolyte management, protein supplementation, antibiotic treatment of C. difficile, and surgical evaluation should be instituted as clinically indicated.

    Hemolytic Anemia

    An immune mediated haemolytic anemia has been observed in patients receiving cephalosporin class antibacterials including ceftriaxone. Severe cases of hemolytic anemia, including fatalities, have been reported during treatment in both adults and children. If a patient develops anemia while on ceftriaxone, the diagnosis of cephalosporin associated anemia should be considered and ceftriaxone stopped until the etiology is determined. 

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  • PRECAUTIONS

    General

    Prescribing ceftriaxone in the absence of a proven or strongly suspected bacterial infection or a prophylactic indication is unlikely to provide benefit to the patient and increases the risk of the development of drug-resistant bacteria.

    Although transient elevations of BUN and serum creatinine have been observed, at the recommended dosages, the nephrotoxic potential of ceftriaxone is similar to that of other cephalosporins.

    Ceftriaxone is excreted via both biliary and renal excretion (see CLINICAL PHARMACOLOGY). Therefore, patients with renal failure normally require no adjustment in dosage when usual doses of ceftriaxone are administered.

    Dosage adjustments should not be necessary in patients with hepatic dysfunction; however, in patients with both hepatic dysfunction and significant renal disease, caution should be exercised and the ceftriaxone dosage should not exceed 2 gm daily.

    Alterations in prothrombin times have occurred rarely in patients treated with ceftriaxone. Patients with impaired vitamin K synthesis or low vitamin K stores (e.g., chronic hepatic disease and malnutrition) may require monitoring of prothrombin time during ceftriaxone treatment. Vitamin K administration (10 mg weekly) may be necessary if the prothrombin time is prolonged before or during therapy.

    Prolonged use of ceftriaxone may result in overgrowth of nonsusceptible organisms. Careful observation of the patient is essential. If superinfection occurs during therapy, appropriate measures should be taken.

    Ceftriaxone should be prescribed with caution in individuals with a history of gastrointestinal disease, especially colitis.

    There have been reports of sonographic abnormalities in the gallbladder of patients treated with ceftriaxone; some of these patients also had symptoms of gallbladder disease. These abnormalities appear on sonography as an echo without acoustical shadowing suggesting sludge or as an echo with acoustical shadowing which may be misinterpreted as gallstones. The chemical nature of the sonographically detected material has been determined to be predominantly a ceftriaxone-calcium salt. The condition appears to be transient and reversible upon discontinuation of ceftriaxone and institution of conservative management. Therefore, ceftriaxone should be discontinued in patients who develop signs and symptoms suggestive of gallbladder disease and/or the sonographic findings described above.

    Cases of pancreatitis possibly secondary to biliary obstruction, have been reported rarely in patients treated with ceftriaxone. Most patients presented with risk factors for biliary stasis and biliary sludge (preceding major therapy, severe illness, total parenteral nutrition). A cofactor role of ceftriaxone-related biliary precipitation cannot be ruled out.

    Information for Patients

    Patients should be counseled that antibacterial drugs including ceftriaxone should only be used to treat bacterial infections. They do not treat viral infections (e.g., common cold). When ceftriaxone is prescribed to treat a bacterial infection, patients should be told that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed. Skipping doses or not completing the full course of therapy may (1) decrease the effectiveness of the immediate treatment and (2) increase the likelihood that bacteria will develop resistance and will not be treatable by ceftriaxone or other antibacterial drugs in the future.

    Diarrhea is a common problem caused by antibiotics which usually ends when the antibiotic is discontinued. Sometimes after starting treatment with antibiotics, patients can develop watery and bloody stools (with or without stomach cramps and fever) even as late as two or more months after having taken the last dose of the antibiotic. If this occurs, patients should contact their physician as soon as possible.

    Carcinogenesis, Mutagenesis, Impairment of Fertility

    Carcinogenesis:

    Considering the maximum duration of treatment and the class of the compound, carcinogenicity studies with ceftriaxone in animals have not been performed. The maximum duration of animal toxicity studies was 6 months.

    Mutagenesis:

    Genetic toxicology tests included the Ames test, a micronucleus test and a test for chromosomal aberrations in human lymphocytes cultured in vitro with ceftriaxone. Ceftriaxone showed no potential for mutagenic activity in these studies.

    Impairment of Fertility:

    Ceftriaxone produced no impairment of fertility when given intravenously to rats at daily doses up to 586 mg/kg/day, approximately 20 times the recommended clinical dose of 2 gm/day.

    Pregnancy

    Teratogenic Effects

    Pregnancy Category B. Reproductive studies have been performed in mice and rats at doses up to 20 times the usual human dose and have no evidence of embryotoxicity, fetotoxicity or teratogenicity. In primates, no embryotoxicity or teratogenicity was demonstrated at a dose approximately 3 times the human dose.

    There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproductive studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

    Nonteratogenic Effects:

    In rats, in the Segment I (fertility and general reproduction) and Segment III (perinatal and postnatal) studies with intravenously administered ceftriaxone, no adverse effects were noted on various reproductive parameters during gestation and lactation, including postnatal growth, functional behavior and reproductive ability of the offspring, at doses of 586 mg/kg/day or less.

    Nursing Mothers

    Low concentrations of ceftriaxone are excreted in human milk. Caution should be exercised when ceftriaxone is administered to a nursing woman.

    Pediatric Use

    Safety and effectiveness of ceftriaxone in neonates, infants and pediatric patients have been established for the dosages described in the DOSAGE AND ADMINISTRATION section. In vitro studies have shown that ceftriaxone, like some other cephalosporins, can displace bilirubin from serum albumin. Ceftriaxone should not be administered to hyperbilirubinemic neonates, especially prematures (see CONTRAINDICATIONS).

    Geriatric Use

    Of the total number of subjects in clinical studies of ceftriaxone, 32% were 60 and over. No overall differences in safety or effectiveness were observed between these subjects and younger subjects, and other reported clinical experience has not identified differences in responses between the elderly and younger patients, but greater sensitivity of some older individuals cannot be ruled out.

    The pharmacokinetics of ceftriaxone were only minimally altered in geriatric patients compared to healthy adult subjects and dosage adjustments are not necessary for geriatric patients with ceftriaxone dosages up to 2 grams per day (see CLINICAL PHARMACOLOGY

    Close
  • ADVERSE REACTIONS

    Ceftriaxone is generally well tolerated. In clinical trials, the following adverse reactions, which were considered to be related to ceftriaxone therapy or of uncertain etiology, were observed:

    LOCAL REACTIONS – pain, induration and tenderness was 1% overall. Phlebitis was reported in < 1% after IV administration. The incidence of warmth, tightness or induration was 17% (3/17) after IM administration of 350 mg/mL and 5% (1/20) after IM administration of 250 mg/mL.

    HYPERSENSITIVITY – rash (1.7%). Less frequently reported (< 1%) were pruritus, fever or chills.

    HEMATOLOGIC – eosinophilia (6%), thrombocytosis (5.1%) and leukopenia (2.1%). Less frequently reported (< 1%) were anemia, hemolytic anemia, neutropenia, lymphopenia, thrombocytopenia and prolongation of the prothrombin time.

    GASTROINTESTINAL – diarrhea (2.7%). Less frequently reported (< 1%) were nausea or vomiting, and dysgeusia. The onset of pseudomembranous colitis symptoms may occur during or after antibacterial treatment (see WARNINGS).

    HEPATIC – elevations of SGOT (3.1%) or SGPT (3.3%). Less frequently reported (< 1%) were elevations of alkaline phosphatase and bilirubin.

    RENAL – elevations of the BUN (1.2%). Less frequently reported (< 1%) were elevations of creatinine and the presence of casts in the urine.

    CENTRAL NERVOUS SYSTEM – headache or dizziness were reported occasionally (< 1%).

    GENITOURINARY – moniliasis or vaginitis were reported occasionally (< 1%).

    MISCELLANEOUS – diaphoresis and flushing were reported occasionally (< 1%).

    Other rarely observed adverse reactions (< 0.1%) include abdominal pain, agranulocytosis, allergic pneumonitis, anaphylaxis, basophilia, biliary lithiasis, bronchospasm, colitis, dyspepsia, epistaxis, flatulence, gallbladder sludge, glycosuria, hematuria, jaundice, leukocytosis, lymphocytosis, monocytosis, nephrolithiasis, palpitations, a decrease in the prothrombin time, renal precipitations, seizures, and serum sickness.

    Post-marketing Experience

    In addition to the adverse reactions reported during clinical trials, the following adverse experiences have been reported during clinical practice in patients treated with ceftriaxone. Data are generally insufficient to allow an estimate of incidence or to establish causation.

    A small number of cases of fatal outcomes in which a crystalline material was observed in the lungs and kidneys at autopsy have been reported in neonates receiving ceftriaxone and calcium-containing fluids. In some of these cases, the same intravenous infusion line was used for both ceftriaxone and calcium‑containing fluids and in some a precipitate was observed in the intravenous infusion line. At least one fatality has been reported in a neonate in whom ceftriaxone and calcium‑containing fluids were administered at different time points via different intravenous lines; no crystalline material was observed at autopsy in this neonate. There have been no similar reports in patients other than neonates.

    GASTROINTESTINAL – stomatitis and glossitis.

    GENITOURINARY – oliguria.

    DERMATOLOGIC – exanthema, allergic dermatitis, urticaria, edema. As with many medications, isolated cases of severe cutaneous adverse reactions (erythema multiforme, Stevens-Johnson syndrome or Lyell’s syndrome/toxic epidermal necrolysis) have been reported.

    Cephalosporin Class Adverse Reactions

    In addition to the adverse reactions listed above which have been observed in patients treated with ceftriaxone, the following adverse reactions and altered laboratory test results have been reported for cephalosporin class antibiotics:

    Adverse Reactions: Allergic reactions, drug fever, serum sickness-like reaction, renal dysfunction, toxic nephropathy, reversible hyperactivity, hypertonia, hepatic dysfunction including cholestasis, aplastic anemia, hemorrhage, and superinfection.

    Altered Laboratory Tests: Positive direct Coombs’ test, false-positive test for urinary glucose, and elevated LDH.

    Several cephalosporins have been implicated in triggering seizures, particularly in patients with renal impairment when the dosage was not reduced (see DOSAGE AND ADMINISTRATION). If seizures associated with drug therapy occur, the drug should be discontinued. Anticonvulsant therapy can be given if clinically indicated.

    To report SUSPECTED ADVERSE REACTIONS, contact West-Ward Pharmaceutical Corp. at 1-877-233-2001 or the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    Close
  • OVERDOSAGE

    In the case of overdosage, drug concentration would not be reduced by hemodialysis or peritoneal dialysis. There is no specific antidote. Treatment of overdosage should be symptomatic.

    Close
  • DOSAGE AND ADMINISTRATION

    Ceftriaxone may be administered intravenously or intramuscularly.

    Do not use diluents containing calcium, such as Ringer’s solution or Hartmann’s solution, to reconstitute ceftriaxone vials or to further dilute a reconstituted vial for IV administration because a precipitate can form. Precipitation of ceftriaxone-calcium can also occur when ceftriaxone is mixed with calcium-containing solutions in the same IV administration line. Ceftriaxone must not be administered simultaneously with calcium‑containing IV solutions, including continuous calcium-containing infusions such as parenteral nutrition via a Y-site. However, in patients other than neonates, ceftriaxone and calcium-containing solutions may be administered sequentially of one another if the infusion lines are thoroughly flushed between infusions with a compatible fluid (see WARNINGS).

    There have been no reports of an interaction between ceftriaxone and oral calcium-containing products or interaction between intramuscular ceftriaxone and calcium-containing products (IV or oral).

    NEONATES

    Hyperbilirubinemic neonates, especially prematures, should not be treated with ceftriaxone (see CONTRAINDICATIONS).

    Ceftriaxone is contraindicated in neonates if they require (or are expected to require) treatment with calcium‑containing IV solutions, including continuous calcium‑containing infusions such as parenteral nutrition because of the risk of precipitation of ceftriaxone-calcium (see CONTRAINDICATIONS).

    PEDIATRIC PATIENTS

    For the treatment of skin and skin structure infections, the recommended total daily dose is 50 to 75 mg/kg given once a day (or in equally divided doses twice a day). The total daily dose should not exceed 2 grams.

    For the treatment of acute bacterial otitis media, a single intramuscular dose of 50 mg/kg (not to exceed 1 gram) is recommended (see INDICATIONS AND USAGE).

    For the treatment of serious miscellaneous infections other than meningitis, the recommended total daily dose is 50 to 75 mg/kg, given in divided doses every 12 hours. The total daily dose should not exceed 2 grams.

    In the treatment of meningitis, it is recommended that the initial therapeutic dose be 100 mg/kg (not to exceed 4 grams). Thereafter, a total daily dose of 100 mg/‌kg/‌day (not to exceed 4 grams daily) is recommended. The daily dose may be administered once a day (or in equally divided doses every 12 hours). The usual duration of therapy is 7 to 14 days.

    ADULTS 

    The usual adult daily dose is 1 to 2 grams given once a day (or in equally divided doses twice a day) depending on the type and severity of infection. For infections caused by Staphylococcus aureus (MSSA), the recommended daily dose is 2 to 4 grams, in order to achieve > 90% target attainment. The total daily dose should not exceed 4 grams.

    If Chlamydia trachomatis is a suspected pathogen, appropriate antichlamydial coverage should be added, because ceftriaxone sodium has no activity against this organism.

    For the treatment of uncomplicated gonococcal infections, a single intramuscular dose of 250 mg is recommended.

    For preoperative use (surgical prophylaxis), a single dose of 1 gram administered intravenously 1/2 to 2 hours before surgery is recommended.

    Generally, ceftriaxone therapy should be continued for at least 2 days after the signs and symptoms of infection have disappeared. The usual duration of therapy is 4 to 14 days; in complicated infections, longer therapy may be required.

    When treating infections caused by Streptococcus pyogenes, therapy should be continued for at least 10 days.

    No dosage adjustment is necessary for patients with impairment of renal or hepatic function.

    DIRECTIONS FOR USE

    Intramuscular Administration: Reconstitute ceftriaxone powder with the appropriate diluent (see COMPATIBILITY AND STABILITY).

    Inject diluent into vial, shake vial thoroughly to form solution. Withdraw entire contents of vial into syringe to equal total labeled dose.

    After reconstitution, each 1 mL of solution contains approximately 250 mg or 350 mg equivalent of ceftriaxone according to the amount of diluent indicated below. If required, more dilute solutions could be utilized. A 350 mg/mL concentration is not recommended for the 250 mg vial since it may not be possible to withdraw the entire contents.

    As with all intramuscular preparations, ceftriaxone should be injected well within the body of a relatively large muscle; aspiration helps to avoid unintentional injection into a blood vessel.

     Vial Dosage Size  Amount of Diluent to be Added
      250 mg/mL  350 mg/mL 

    250 mg

    0.9 mL

    500 mg

    1.8 mL

    1.0 mL

    1 gm

    3.6 mL

    2.1 mL

    2 gm

    7.2 mL

    4.2 mL

    Intravenous Administration: Ceftriaxone should be administered intravenously by infusion over a period of 30 minutes. Concentrations between 10 mg/mL and 40 mg/‌mL are recommended; however, lower concentrations may be used if desired. Reconstitute vials with an appropriate IV diluent (see COMPATIBILITY AND STABILITY).

    Vial Dosage Size

      Amount of Diluent to be Added

    250 mg

    2.4 mL

    500 mg

    4.8 mL

    1 gm

    9.6 mL

    2 gm

    19.2 mL

    After reconstitution, each 1 mL of solution contains approximately 100 mg equivalent of ceftriaxone. Withdraw entire contents and dilute to the desired concentration with the appropriate IV diluent.

    Close
  • COMPATIBILITY AND STABILITY

    Ceftriaxone has been shown to be compatible with Flagyl® IV (metronidazole hydrochloride). The concentration should not exceed 5 to 7.5 mg/mL metronidazole hydrochloride with ceftriaxone 10 mg/mL as an admixture. The admixture is stable for 24 hours at room temperature only in 0.9% sodium chloride injection or 5% dextrose in water (D5W). No compatibility studies have been conducted with the Flagyl® IV RTU® (metronidazole) formulation or using other diluents. Metronidazole at concentrations greater than 8 mg/mL will precipitate. Do not refrigerate the admixture as precipitation will occur.

    Vancomycin, amsacrine, aminoglycosides, and fluconazole are physically incompatible with ceftriaxone in admixtures. When any of these drugs are to be administered concomitantly with ceftriaxone by intermittent intravenous infusion, it is recommended that they be given sequentially, with thorough flushing of the intravenous lines (with one of the compatible fluids) between the administrations.

    Do not use diluents containing calcium, such as Ringer’s solution or Hartmann’s solution, to reconstitute ceftriaxone vials or to further dilute a reconstituted vial for IV administration. Particulate formation can result.

    Ceftriaxone solutions should not be physically mixed with or piggybacked into solutions containing other antimicrobial drugs or into diluent solutions other than those listed above, due to possible incompatibility (see WARNINGS).

    Ceftriaxone sterile powder should be stored at 20º to 25ºC (68º to 77ºF) [see USP Controlled Room Temperature] and protected from light. After reconstitution, protection from normal light is not necessary. The color of solutions ranges from light yellow to amber, depending on the length of storage, concentration and diluent used.

    Ceftriaxone intramuscular solutions remain stable (loss of potency less than 10%) for the following time periods:

    Diluent

    Concentration
    mg/mL

    Storage

    Room Temp.
    (25°C)

    Refrigerated
    (4°C)

    Sterile Water for Injection

    100

    2 days

    10 days

    250, 350

    24 hours

    3 days

    0.9% Sodium Chloride Solution

    100

    2 days

    10 days

    250, 350

    24 hours

    3 days

    5% Dextrose Solution

    100

    2 days

    10 days

    250, 350

    24 hours

    3 days

    Bacteriostatic Water + 0.9% Benzyl Alcohol

    100

    24 hours

    10 days

    250, 350

    24 hours

    3 days

    1% Lidocaine Solution (without epinephrine)

    100

    24 hours

    10 days

     

    250, 350

    24 hours

    3 days

    Ceftriaxone intravenous solutions, at concentrations of 10, 20 and 40 mg/mL, remain stable (loss of potency less than 10%) for the following time periods stored in glass or PVC containers:

      Storage
     Diluent Room Temp.  Refrigerated 
      (25ºC) (4ºC)
     Sterile Water  2 days 10 days 
     0.9% Sodium Chloride Solution  2 days  10 days
     5% Dextrose Solution  2 days  10 days
     10% Dextrose Solution  2 days  10 days
     5% Dextrose + 0.9% Sodium Chloride Solution*  2 days  Incompatible
     5% Dextrose + 0.45% Sodium Chloride Solution  2 days  Incompatible

     *Data available for 10 to 40 mg/mL concentrations in this diluent in PVC containers only.

    The following intravenous ceftriaxone solutions are stable at room temperature (25°C) for 24 hours, at concentrations between 10 mg/mL and 40 mg/mL: Sodium Lactate (PVC container), 10% Invert Sugar (glass container), 5% Sodium Bicarbonate (glass container), Freamine III (glass container), Normosol-M in 5% Dextrose (glass and PVC containers), Ionosol-B in 5% Dextrose (glass container), 5% Mannitol (glass container), 10% Mannitol (glass container).

    After the indicated stability time periods, unused portions of solutions should be discarded.

    NOTE: Parenteral drug products should be inspected visually for particulate matter before administration.

    Ceftriaxone reconstituted with 5% Dextrose or 0.9% Sodium Chloride solution at concentrations between 10 mg/‌mL and 40 mg/mL, and then stored in frozen state (- 20°C) in PVC or polyolefin containers, remains stable for 26 weeks.

    Frozen solutions of ceftriaxone should be thawed at room temperature before use. After thawing, unused portions should be discarded. DO NOT REFREEZE.

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  • ANIMAL PHARMACOLOGY

    Concretions consisting of the precipitated calcium salt of ceftriaxone have been found in the gallbladder bile of dogs and baboons treated with ceftriaxone.

    These appeared as a gritty sediment in dogs that received 100 mg/kg/day for 4 weeks. A similar phenomenon has been observed in baboons but only after a protracted dosing period (6 months) at higher dose levels (335 mg/kg/day or more). The likelihood of this occurrence in humans is considered to be low, since ceftriaxone has a greater plasma half-life in humans, the calcium salt of ceftriaxone is more soluble in human gallbladder bile and the calcium content of human gallbladder bile is relatively low.

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  • HOW SUPPLIED

    Ceftriaxone for Injection, USP is supplied as a sterile crystalline powder in glass vials. The following packages are available:

    Vials containing ceftriaxone sodium equivalent to 250 mg ceftriaxone      Box of 25 (NDC 0143-9859-25)

    Vials containing ceftriaxone sodium equivalent to 500 mg ceftriaxone      Box of 25 (NDC 0143-9858-25)

    Vials containing ceftriaxone sodium equivalent to 1 gm ceftriaxone         Box of 25 (NDC 0143-9857-25)

    Vials containing ceftriaxone sodium equivalent to 2 gm ceftriaxone         Box of 25 (NDC 0143-9856-25)

    Note: Ceftriaxone for Injection, USP sterile powder should be stored at 20º to 25ºC (68º to 77ºF) [See USP Controlled Room Temperature], and protected from light.

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  • CLINICAL STUDIES

    Clinical Trials in Pediatric Patients With Acute Bacterial Otitis Media:  In two adequate and well-controlled US clinical trials a single IM dose of ceftriaxone was compared with a 10 day course of oral antibiotic in pediatric patients between the ages of 3 months and 6 years. The clinical cure rates and statistical outcome appear in the table below:

    Clinical Efficacy in Evaluable Population
    Study Day   Ceftriaxone Single Dose Comparator - 10 Days of Oral Therapy  95% Confidence Interval  Statistical Outcome 
    Study 1 - US    amoxicillin/clavulanate    
     14 74% (220/296)  82% (247/302)  (-14.4%, -0.5%)   Ceftriaxone is lower than control
     28  58% (167/288) 67% (200/297)  (-17.5%, -1.2%)  at study day 14 and 28. 
    Study 2 - US5   TMP-SMZ     
     14 54% (113/210)   60% (124/206) (-16.4%, 3.6%)   Ceftriaxone is equivalent to control
     28 35% (73/206)  45% (93/205)  (-19.9%, 0.0%)  at study day 14 and 28.

    An open-label bacteriologic study of ceftriaxone without a comparator enrolled 108 pediatric patients, 79 of whom had positive baseline cultures for one or more of the common pathogens. The results of this study are tabulated as follows:

    Week 2 and 4 Bacteriologic Eradication Rates in the Per Protocol Analysis in the Roche Bacteriologic Study by pathogen:

       Study Day 13-15  Study Day 30+2
     Organism No. Analyzed   No. Erad. (%) No. Analyzed  No. Erad. (%) 
     Streptococcus pneumoniae  38 32 (84) 35 25 (71)
     Haemophilus influenzae  33 28 (85) 31 22 (71)
     Moraxella catarrhalis  15 12 (80) 15 9 (60)
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  • REFERENCES

    1. Clinical and Laboratory Standards Institute (CLSI). Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria That Grow Aerobically; Approved Standard - Ninth Edition. CLSI document M07-A9. Clinical and Laboratory Standards Institute, 950 West Valley Road, Suite 2500, Wayne, Pennsylvania 19087, USA, 2012.
    2. Clinical and Laboratory Standards Institute (CLSI). Performance Standards for Antimicrobial Susceptibility Testing; Twenty-third Informational Supplement. CLSI document M100-S23. Clinical and Laboratory Standards Institute, 950 West Valley Road, Suite 2500, Pennsylvania 19087, USA, 2013.
    3. Clinical and Laboratory Standards Institute (CLSI). Performance Standards for Antimicrobial Disk Susceptibility Tests; Approved Standard - Eleventh Edition. CLSI document M02-A11. Clinical and Laboratory Standards Institute, 950 West Valley Road, Suite 2500, Wayne, Pennsylvania 19087, USA, 2012.
    4. Clinical and Laboratory Standards Institute (CLSI). Methods for Antimicrobial Susceptibility Testing of Anaerobic Bacteria; Approved Standard - Eight Edition. CLSI document M11-A8. Clinical and Laboratory Standards Institute, 950 West Valley Road, Suite 2500, Wayne, PA 19087 USA, 2012.
    5. Barnett ED, Teele DW, Klein JO, et al. Comparison of Ceftriaxone and Trimethoprim-Sulfamethoxazole for Acute Otitis Media. Pediatrics. Vol. 99, No. 1, January 1997.

    Manufactured by:
    HIKMA FARMACÊUTICA (PORTUGAL), S.A.
    Estrada do Rio da Mó, nº 8, 8A e 8B – Fervença - 2705 – 906 Terrugem SNT, PORTUGAL

    Distributed by:
    WEST-WARD PHARMACEUTICAL CORP.
    Eatontown, NJ 07724 USA

    Revised: 04/2014
    PIN149-WES/5

    Close
  • PRINCIPAL DISPLAY PANEL

    NDC 0143-9859-01
    Rx only
    CEFTRIAXONE
    FOR INJECTION, USP
    250 mg/Vial
    EQUIVALENT TO 250 MG CEFTRIAXONE
    FOR IV OR IM USE

    Single Dose Vial
    PROTECT FROM LIGHT
    A 350 mg/mL concentration is not recom-
    mended for the 250 mg vial since it may
    not be possible to withdraw the entire
    contents.
    For IV or IM administration and
    USUAL
    DOSAGE:
    See package insert.
    Storage Prior to Reconstitution: Store
    powder at 20º to 25ºC (68º to 77ºF) [See
    USP Controlled Room Temperature].
    Storage After Reconstitution: See package
    insert.

    NDC 0143-9859-01 Rx only CEFTRIAXONE FOR INJECTION, USP 250 mg/Vial EQUIVALENT TO 250 MG CEFTRIAXONE FOR IV OR IM USE Single Dose Vial PROTECT FROM LIGHT A 350 mg/mL concentration is not recommended for the 250 mg vial since it may not be possible to withdraw the entire contents. For IV or IM administration and USUAL DOSAGE: See package insert. Storage Prior to Reconstitution: Store powder at 20º to 25ºC (68º to 77ºF) [See USP Controlled Room Temperature]. Storage After Reconstitution: See package insert.
    Close
  • PRINCIPAL DISPLAY PANEL

    NDC 0143-9858-01
    Rx only
    CEFTRIAXONE
    FOR INJECTION, USP
    500 mg/Vial
    EQUIVALENT TO 500 MG CEFTRIAXONE
    FOR IV OR IM USE

    Single Dose Vial
    PROTECT FROM LIGHT
    For IM administration: Reconstitute with 1 mL 1%
    Lidocaine Hydrochloride Injection, USP or Sterile
    Water for Injection, USP. Each 1 mL of solution con-
    tains approximately 350 mg equivalent of ceftriaxone.
    For IV administration: Reconstitute with 4.8 mL of an
    IV diluent specified in the accompanying package
    insert. Each 1 mL of solution contains approximately
    100 mg equivalent of ceftriaxone. Withdraw entire
    contents and dilute to the desired concentration with
    the appropriate IV diluent.
    USUAL DOSAGE and Storage After Reconstitution:
    See package insert. ​​​​​​​​Storage Prior to Reconstitution:
    Store powder at 20º to 25ºC (68º to 77ºF) [See USP
    Controlled Room Temperature].

    NDC 0143-9858-01 Rx only CEFTRIAXONE FOR INJECTION, USP 500 mg/Vial EQUIVALENT TO 500 MG CEFTRIAXONE FOR IV OR IM USE Single Dose Vial PROTECT FROM LIGHT For IM administration: Reconstitute with 1 mL 1% Lidocaine Hydrochloride Injection, USP or Sterile Water for Injection, USP. Each 1 mL of solution con- tains approximately 350 mg equivalent of ceftriaxone. For IV administration: Reconstitute with 4.8 mL of an IV diluent specified in the accompanying package insert. Each 1 mL of solution contains approximately 100 mg equivalent of ceftriaxone. Withdraw entire contents and dilute to the desired concentration with the appropriate IV diluent. USUAL DOSAGE and Storage After Reconstitution: See package insert. ​​​​​​​​Storage Prior to Reconstitution: Store powder at 20º to 25ºC (68º to 77ºF) [See USP Controlled Room Temperature].

    Close
  • PRINCIPAL DISPLAY PANEL

    NDC 0143-9857-01
    Rx only
    CEFTRIAXONE
    FOR INJECTION, USP
    1 gram/Vial
    EQUIVALENT TO 1 GRAM CEFTRIAXONE
    FOR IV OR IM USE

    Single Dose Vial
    PROTECT FROM LIGHT
    For IM administration: Reconstitute with 2.1 mL 1%
    Lidocaine Hydrochloride Injection, USP or Sterile
    Water for Injection, USP. Each 1 mL of solution con-
    tains approximately 350 mg equivalent of ceftriaxone.
    For IV administration: Reconstitute with 9.6 mL of an
    IV diluent specified in the accompanying package
    insert. Each 1 mL of solution contains approximately
    100 mg equivalent of ceftriaxone. Withdraw entire
    contents and dilute to the desired concentration with
    the appropriate IV diluent.
    USUAL DOSAGE and Storage After Reconstitution:
    See package insert. Storage Prior to Reconstitution:
    Store powder at 20º to 25ºC (68º to 77ºF) [See USP
    Controlled Room Temperature].

    NDC 0143-9857-01 Rx only CEFTRIAXONE FOR INJECTION, USP 1 gram/Vial EQUIVALENT TO 1 GRAM CEFTRIAXONE FOR IV OR IM USE Single Dose Vial PROTECT FROM LIGHT For IM administration: Reconstitute with 2.1 mL 1% Lidocaine Hydrochloride Injection, USP or Sterile Water for Injection, USP. Each 1 mL of solution contains approximately 350 mg equivalent of ceftriaxone. For IV administration: Reconstitute with 9.6 mL of an IV diluent specified in the accompanying package insert. Each 1 mL of solution contains approximately 100 mg equivalent of ceftriaxone. Withdraw entire contents and dilute to the desired concentration with the appropriate IV diluent. USUAL DOSAGE and Storage After Reconstitution: See package insert. Storage Prior to Reconstitution: Store powder at 20º to 25ºC (68º to 77ºF) [See USP Controlled Room Temperature].
    Close
  • PRINCIPAL DISPLAY PANEL

    NDC 0143-9856-01
    Rx only
    CEFTRIAXONE
    FOR INJECTION, USP
    2 grams/Vial
    EQUIVALENT TO 2 GRAMS CEFTRIAXONE
    FOR IV OR IM USE

    Single Dose Vial
    PROTECT FROM LIGHT
    For IM administration: Reconstitute with 4.2 mL 1%
    Lidocaine Hydrochloride Injection, USP or Sterile
    Water for Injection, USP. Each 1 mL of solution con-
    tains approximately 350 mg equivalent of ceftriaxone.
    For IV administration: Reconstitute with 19.2 mL of
    an IV diluent specified in the accompanying package
    insert. Each 1 mL of solutin contains approximately
    100 mg equivalent of ceftriaxone. Withdraw entire
    contents and dilute to the desired concentration with
    the appropriate IV diluent.
    USUAL DOSAGE and Storage After Reconstitution:
    See package insert. Storage Prior to Reconstitution:
    Store powder at 20º to 25ºC (68º to 77ºF) [See USP
    Controlled Room Temperature].

    NDC 0143-9856-01 Rx only CEFTRIAXONE FOR INJECTION, USP 2 grams/Vial EQUIVALENT TO 2 GRAMS CEFTRIAXONE FOR IV OR IM USE Single Dose Vial PROTECT FROM LIGHT For IM administration: Reconstitute with 4.2 mL 1% Lidocaine Hydrochloride Injection, USP or Sterile Water for Injection, USP. Each 1 mL of solution contains approximately 350 mg equivalent of ceftriaxone. For IV administration: Reconstitute with 19.2 mL of an IV diluent specified in the accompanying package insert. Each 1 mL of solutin contains approximately 100 mg equivalent of ceftriaxone. Withdraw entire contents and dilute to the desired concentration with the appropriate IV diluent. USUAL DOSAGE and Storage After Reconstitution: See package insert. Storage Prior to Reconstitution: Store powder at 20º to 25ºC (68º to 77ºF) [See USP Controlled Room Temperature]. 

    Close
  • INGREDIENTS AND APPEARANCE
    CEFTRIAXONE 
    ceftriaxone injection, powder, for solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0143-9859
    Route of Administration INTRAMUSCULAR, INTRAVENOUS DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CEFTRIAXONE SODIUM (CEFTRIAXONE) CEFTRIAXONE 250 mg
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0143-9859-25 25 in 1 BOX
    1 NDC:0143-9859-01 1 in 1 VIAL
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA065342 01/10/2008
    CEFTRIAXONE 
    ceftriaxone injection, powder, for solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0143-9858
    Route of Administration INTRAMUSCULAR, INTRAVENOUS DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CEFTRIAXONE SODIUM (CEFTRIAXONE) CEFTRIAXONE 500 mg
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0143-9858-25 25 in 1 BOX
    1 NDC:0143-9858-01 1 in 1 VIAL
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA065342 01/10/2008
    CEFTRIAXONE 
    ceftriaxone injection, powder, for solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0143-9857
    Route of Administration INTRAMUSCULAR, INTRAVENOUS DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CEFTRIAXONE SODIUM (CEFTRIAXONE) CEFTRIAXONE 1 g
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0143-9857-25 25 in 1 BOX
    1 NDC:0143-9857-01 1 in 1 VIAL
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA065342 01/10/2008
    CEFTRIAXONE 
    ceftriaxone injection, powder, for solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0143-9856
    Route of Administration INTRAMUSCULAR, INTRAVENOUS DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CEFTRIAXONE SODIUM (CEFTRIAXONE) CEFTRIAXONE 2 g
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0143-9856-25 25 in 1 BOX
    1 NDC:0143-9856-01 1 in 1 VIAL
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA065342 01/10/2008
    Labeler - West-Ward Pharmaceutical Corp (001230762)
    Establishment
    Name Address ID/FEI Business Operations
    HIKMA FARMACEUTICA (PORTUGAL), S.A 452742943 ANALYSIS(0143-9859, 0143-9858, 0143-9857, 0143-9856), LABEL(0143-9859, 0143-9858, 0143-9857, 0143-9856), MANUFACTURE(0143-9859, 0143-9858, 0143-9857, 0143-9856), PACK(0143-9859, 0143-9858, 0143-9857, 0143-9856)
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