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    NDC 42571-0334-01 Metformin Hydrochloride 1000 mg/1 Details

    Metformin Hydrochloride 1000 mg/1

    Metformin Hydrochloride is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Micro Labs Limited. The primary component is METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 42571-0334
    Product ID 42571-334_f20dafcf-7ee0-3608-e053-2995a90a8c47
    Associated GPIs
    GCN Sequence Number 061273
    GCN Sequence Number Description metformin HCl TABERGR24H 1000 MG ORAL
    HIC3 C4L
    HIC3 Description ANTIHYPERGLYCEMIC, BIGUANIDE TYPE
    GCN 97067
    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 1000
    Active Ingredient Units mg/1
    Substance Name METFORMIN HYDROCHLORIDE
    Labeler Name Micro Labs Limited
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA212448
    Listing Certified Through 2024-12-31

    Package

    NDC 42571-0334-01 (42571033401)

    NDC Package Code 42571-334-01
    Billing NDC 42571033401
    Package 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42571-334-01)
    Marketing Start Date 2023-03-01
    NDC Exclude Flag N
    Pricing Information N/A