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    NDC 68462-0520-10 METFORMIN HYDROCHLORIDE 500 mg/1 Details

    METFORMIN HYDROCHLORIDE 500 mg/1

    METFORMIN HYDROCHLORIDE is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by GLENMARK PHARMACEUTICALS INC., USA. The primary component is METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 68462-0520
    Product ID 68462-520_ef160cca-85e2-440c-997f-0535914b4d3f
    Associated GPIs 27250050007580
    GCN Sequence Number 061267
    GCN Sequence Number Description metformin HCl TABERGR24H 500 MG ORAL
    HIC3 C4L
    HIC3 Description ANTIHYPERGLYCEMIC, BIGUANIDE TYPE
    GCN 97061
    HICL Sequence Number 004763
    HICL Sequence Number Description METFORMIN HCL
    Brand/Generic Generic
    Proprietary Name METFORMIN HYDROCHLORIDE
    Proprietary Name Suffix n/a
    Non-Proprietary Name metformin hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name METFORMIN HYDROCHLORIDE
    Labeler Name GLENMARK PHARMACEUTICALS INC., USA
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA212969
    Listing Certified Through 2025-12-31

    Package

    NDC 68462-0520-10 (68462052010)

    NDC Package Code 68462-520-10
    Billing NDC 68462052010
    Package 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-520-10)
    Marketing Start Date 2019-11-25
    NDC Exclude Flag N
    Pricing Information N/A