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    NDC 70518-3260-00 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 REMEDYREPACK INC.. The primary component is METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 70518-3260
    Product ID 70518-3260_06bbf597-92af-0d04-e063-6294a90a8abc
    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 ER
    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 REMEDYREPACK INC.
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA201991
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3260-00 (70518326000)

    NDC Package Code 70518-3260-0
    Billing NDC 70518326000
    Package 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3260-0)
    Marketing Start Date 2021-10-30
    NDC Exclude Flag N
    Pricing Information N/A