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    NDC 33342-0141-11 Metformin hydrochloride 500 mg/1 Details

    Metformin hydrochloride 500 mg/1

    Metformin hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Macleods Pharmaceuticals Limited. The primary component is METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 33342-0141
    Product ID 33342-141_3ce6010c-10dd-4e6f-9517-d71c0489a7c5
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name METFORMIN HYDROCHLORIDE
    Labeler Name Macleods Pharmaceuticals Limited
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA205330
    Listing Certified Through 2024-12-31

    Package

    NDC 33342-0141-11 (33342014111)

    NDC Package Code 33342-141-11
    Billing NDC 33342014111
    Package 100 TABLET, FILM COATED in 1 BOTTLE (33342-141-11)
    Marketing Start Date 2017-11-01
    NDC Exclude Flag N
    Pricing Information N/A