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    NDC 68788-7901-01 METFORMIN HYDROCHLORIDE 850 mg/1 Details

    METFORMIN HYDROCHLORIDE 850 mg/1

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

    Product Information

    NDC 68788-7901
    Product ID 68788-7901_7a56529d-adf5-4db7-9433-8acd3c0813cb
    Associated GPIs 27250050000340
    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
    Route ORAL
    Active Ingredient Strength 850
    Active Ingredient Units mg/1
    Substance Name METFORMIN HYDROCHLORIDE
    Labeler Name Preferred Pharmaceuticals 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 68788-7901-01 (68788790101)

    NDC Package Code 68788-7901-1
    Billing NDC 68788790101
    Package 100 TABLET in 1 BOTTLE (68788-7901-1)
    Marketing Start Date 2021-05-14
    NDC Exclude Flag N
    Pricing Information N/A