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    NDC 67877-0218-10 Metformin Hydrochloride 850 mg/1 Details

    Metformin Hydrochloride 850 mg/1

    Metformin Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Ascend Laboratories, LLC. The primary component is METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 67877-0218
    Product ID 67877-218_fe84bb3e-625a-4eff-8df0-6bbaa6548920
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 850
    Active Ingredient Units mg/1
    Substance Name METFORMIN HYDROCHLORIDE
    Labeler Name Ascend Laboratories, LLC
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA091184
    Listing Certified Through 2024-12-31

    Package

    NDC 67877-0218-10 (67877021810)

    NDC Package Code 67877-218-10
    Billing NDC 67877021810
    Package 1000 TABLET, FILM COATED in 1 BOTTLE (67877-218-10)
    Marketing Start Date 2011-01-31
    NDC Exclude Flag N
    Pricing Information N/A