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    NDC 17224-0318-21 Metformin Hydrochloride 500 mg/1 Details

    Metformin Hydrochloride 500 mg/1

    Metformin Hydrochloride is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Calvin Scott & Co., Inc.. The primary component is METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 17224-0318
    Product ID 17224-318_f99bf123-ea91-ced5-e053-6294a90a7715
    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, COATED
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name METFORMIN HYDROCHLORIDE
    Labeler Name Calvin Scott & Co., Inc.
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA205096
    Listing Certified Through 2024-12-31

    Package

    NDC 17224-0318-21 (17224031821)

    NDC Package Code 17224-318-21
    Billing NDC 17224031821
    Package 21 TABLET, COATED in 1 BOTTLE (17224-318-21)
    Marketing Start Date 2019-05-01
    NDC Exclude Flag N
    Pricing Information N/A