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    NDC 71335-0720-01 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 Bryant Ranch Prepack. The primary component is METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 71335-0720
    Product ID 71335-0720_9f06ac77-2411-4c32-bbed-47cb6dcdbfb9
    Associated GPIs 27250050007520
    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 Bryant Ranch Prepack
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078321
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-0720-01 (71335072001)

    NDC Package Code 71335-0720-1
    Billing NDC 71335072001
    Package 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-1)
    Marketing Start Date 2018-03-15
    NDC Exclude Flag N
    Pricing Information N/A