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    NDC 47335-0306-83 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 Sun Pharmaceutical Industries, Inc.. The primary component is METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 47335-0306
    Product ID 47335-306_33ab529d-b535-4138-9c3d-dbde05d702c9
    Associated GPIs 27250050007590
    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 Sun Pharmaceutical Industries, Inc.
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202917
    Listing Certified Through 2025-12-31

    Package

    NDC 47335-0306-83 (47335030683)

    NDC Package Code 47335-306-83
    Billing NDC 47335030683
    Package 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-83)
    Marketing Start Date 2018-05-22
    NDC Exclude Flag N
    Pricing Information N/A