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    NDC 63739-0900-26 Heparin Sodium 1000 [USP'U]/mL Details

    Heparin Sodium 1000 [USP'U]/mL

    Heparin Sodium is a INTRAVENOUS; SUBCUTANEOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by McKesson Corporation dba SKY Packaging. The primary component is HEPARIN SODIUM.

    Product Information

    NDC 63739-0900
    Product ID 63739-900_041f4c70-eb0b-e76e-e063-6394a90aaeb4
    Associated GPIs 83100020202015
    GCN Sequence Number 060309
    GCN Sequence Number Description heparin sodium,porcine/PF VIAL 1000/ML INJECTION
    HIC3 M9K
    HIC3 Description HEPARIN AND RELATED PREPARATIONS
    GCN 26429
    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 1000
    Active Ingredient Units [USP'U]/mL
    Substance Name HEPARIN SODIUM
    Labeler Name McKesson Corporation dba SKY Packaging
    Pharmaceutical Class Anti-coagulant [EPC], Heparin [CS], Unfractionated Heparin [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202732
    Listing Certified Through 2024-12-31

    Package

    NDC 63739-0900-26 (63739090026)

    NDC Package Code 63739-900-26
    Billing NDC 63739090026
    Package 25 VIAL, SINGLE-DOSE in 1 CARTON (63739-900-26) / 2 mL in 1 VIAL, SINGLE-DOSE (63739-900-12)
    Marketing Start Date 2014-06-12
    NDC Exclude Flag N
    Pricing Information N/A