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    NDC 00409-1316-32 Heparin Sodium 10000 [USP'U]/mL Details

    Heparin Sodium 10000 [USP'U]/mL

    Heparin Sodium is a INTRAVENOUS; SUBCUTANEOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Hospira, Inc.. The primary component is HEPARIN SODIUM.

    Product Information

    NDC 00409-1316
    Product ID 0409-1316_e616e4ae-b6f6-4769-b770-c03f1198c1b3
    Associated GPIs 83100020202034
    GCN Sequence Number 060312
    GCN Sequence Number Description heparin sodium,porcine/PF CARTRIDGE 5000/0.5ML INJECTION
    HIC3 M9K
    HIC3 Description HEPARIN AND RELATED PREPARATIONS
    GCN 26436
    HICL Sequence Number 033314
    HICL Sequence Number Description HEPARIN SODIUM,PORCINE/PF
    Brand/Generic Generic
    Proprietary Name Heparin Sodium
    Proprietary Name Suffix n/a
    Non-Proprietary Name HEPARIN SODIUM
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAVENOUS; SUBCUTANEOUS
    Active Ingredient Strength 10000
    Active Ingredient Units [USP'U]/mL
    Substance Name HEPARIN SODIUM
    Labeler Name Hospira, Inc.
    Pharmaceutical Class Anti-coagulant [EPC], Heparin [CS], Unfractionated Heparin [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA089522
    Listing Certified Through 2024-12-31

    Package

    NDC 00409-1316-32 (00409131632)

    NDC Package Code 0409-1316-32
    Billing NDC 00409131632
    Package 50 CARTRIDGE in 1 CONTAINER (0409-1316-32) / .5 mL in 1 CARTRIDGE (0409-1316-11)
    Marketing Start Date 2005-03-31
    NDC Exclude Flag N
    Pricing Information N/A