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    NDC 70518-1951-01 Metformin Hydrochloride 500 mg/1 Details

    Metformin Hydrochloride 500 mg/1

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

    Product Information

    NDC 70518-1951
    Product ID 70518-1951_f6514a42-bf0e-5d85-e053-2995a90a00ae
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 500
    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 ANDA203769
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-1951-01 (70518195101)

    NDC Package Code 70518-1951-1
    Billing NDC 70518195101
    Package 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1951-1)
    Marketing Start Date 2021-05-04
    NDC Exclude Flag N
    Pricing Information N/A