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    NDC 72578-0035-05 Metformin Hydrochloride 500 mg/1 Details

    Metformin Hydrochloride 500 mg/1

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

    Product Information

    NDC 72578-0035
    Product ID 72578-035_ca52a4c2-f8fd-4395-a307-3c1ec9c3cf7f
    Associated GPIs
    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, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name METFORMIN HYDROCHLORIDE
    Labeler Name Viona Pharmaceuticals Inc
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077060
    Listing Certified Through 2024-12-31

    Package

    NDC 72578-0035-05 (72578003505)

    NDC Package Code 72578-035-05
    Billing NDC 72578003505
    Package 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-035-05)
    Marketing Start Date 2019-03-15
    NDC Exclude Flag N
    Pricing Information N/A