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    NDC 70518-3084-02 Metformin Hydrochloride 850 mg/1 Details

    Metformin Hydrochloride 850 mg/1

    Metformin Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 70518-3084
    Product ID 70518-3084_05a380c7-d11d-f740-e063-6394a90a6109
    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 Metformin Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Metformin Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 850
    Active Ingredient Units mg/1
    Substance Name METFORMIN HYDROCHLORIDE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090564
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3084-02 (70518308402)

    NDC Package Code 70518-3084-2
    Billing NDC 70518308402
    Package 90 TABLET in 1 BOTTLE, PLASTIC (70518-3084-2)
    Marketing Start Date 2022-09-07
    NDC Exclude Flag N
    Pricing Information N/A
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