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    NDC 68180-0339-02 METFORMIN HYDROCHLORIDE 1000 mg/1 Details

    METFORMIN HYDROCHLORIDE 1000 mg/1

    METFORMIN HYDROCHLORIDE is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lupin Pharmaceuticals, Inc.. The primary component is METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 68180-0339
    Product ID 68180-339_28e237fd-5569-4af9-8c15-bed92c928bfa
    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, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 1000
    Active Ingredient Units mg/1
    Substance Name METFORMIN HYDROCHLORIDE
    Labeler Name Lupin Pharmaceuticals, Inc.
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA091664
    Listing Certified Through 2024-12-31

    Package

    NDC 68180-0339-02 (68180033902)

    NDC Package Code 68180-339-02
    Billing NDC 68180033902
    Package 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-339-02)
    Marketing Start Date 2016-02-01
    NDC Exclude Flag N
    Pricing Information N/A