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    NDC 00409-7337-01 Ceftriaxone Sodium 250 mg/1 Details

    Ceftriaxone Sodium 250 mg/1

    Ceftriaxone Sodium is a INTRAMUSCULAR; INTRAVENOUS INJECTION, POWDER, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Hospira, Inc. The primary component is CEFTRIAXONE SODIUM.

    Product Information

    NDC 00409-7337
    Product ID 0409-7337_c89e0cee-3419-4c53-bce1-796a1f911117
    Associated GPIs 02300090102105
    GCN Sequence Number 009165
    GCN Sequence Number Description ceftriaxone sodium VIAL 250 MG INJECTION
    HIC3 W1Y
    HIC3 Description CEPHALOSPORIN ANTIBIOTICS - 3RD GENERATION
    GCN 39960
    HICL Sequence Number 003996
    HICL Sequence Number Description CEFTRIAXONE SODIUM
    Brand/Generic Generic
    Proprietary Name Ceftriaxone Sodium
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ceftriaxone Sodium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, POWDER, FOR SOLUTION
    Route INTRAMUSCULAR; INTRAVENOUS
    Active Ingredient Strength 250
    Active Ingredient Units mg/1
    Substance Name CEFTRIAXONE SODIUM
    Labeler Name Hospira, Inc
    Pharmaceutical Class Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA065169
    Listing Certified Through 2025-12-31

    Package

    NDC 00409-7337-01 (00409733701)

    NDC Package Code 0409-7337-01
    Billing NDC 00409733701
    Package 10 VIAL, SINGLE-USE in 1 CARTON (0409-7337-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7337-11)
    Marketing Start Date 2005-05-09
    NDC Exclude Flag N
    Pricing Information N/A