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    NDC 68083-0640-10 ENOXAPARIN SODIUM 150 mg/mL Details

    ENOXAPARIN SODIUM 150 mg/mL

    ENOXAPARIN SODIUM is a SUBCUTANEOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Gland Pharma Limited. The primary component is ENOXAPARIN SODIUM.

    Product Information

    NDC 68083-0640
    Product ID 68083-640_65025e0d-eb54-4c4e-bd14-f294ce038902
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name ENOXAPARIN SODIUM
    Proprietary Name Suffix n/a
    Non-Proprietary Name ENOXAPARIN SODIUM
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION
    Route SUBCUTANEOUS
    Active Ingredient Strength 150
    Active Ingredient Units mg/mL
    Substance Name ENOXAPARIN SODIUM
    Labeler Name Gland Pharma Limited
    Pharmaceutical Class Heparin, Low-Molecular-Weight [CS], Low Molecular Weight Heparin [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078990
    Listing Certified Through 2024-12-31

    Package

    NDC 68083-0640-10 (68083064010)

    NDC Package Code 68083-640-10
    Billing NDC 68083064010
    Package 10 SYRINGE in 1 CARTON (68083-640-10) / 1 mL in 1 SYRINGE
    Marketing Start Date 2023-07-11
    NDC Exclude Flag N
    Pricing Information N/A