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    NDC 53002-1500-03 METFORMIN HYDROCHLORIDE EXTENDED RELEASE 500 mg/1 Details

    METFORMIN HYDROCHLORIDE EXTENDED RELEASE 500 mg/1

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

    Product Information

    NDC 53002-1500
    Product ID 53002-1500_e0291175-3c5d-4e27-8e89-88d3c0c7b983
    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 EXTENDED RELEASE
    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 RPK Pharmaceuticals, Inc.
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090295
    Listing Certified Through 2024-12-31

    Package

    NDC 53002-1500-03 (53002150003)

    NDC Package Code 53002-1500-3
    Billing NDC 53002150003
    Package 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (53002-1500-3)
    Marketing Start Date 2023-01-01
    NDC Exclude Flag N
    Pricing Information N/A