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    NDC 65862-0009-33 Metformin Hydrochloride 850 mg/1 Details

    Metformin Hydrochloride 850 mg/1

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

    Product Information

    NDC 65862-0009
    Product ID 65862-009_c535450c-12fd-478d-ad45-743c5badfc28
    Associated GPIs 27250050000340
    GCN Sequence Number 016441
    GCN Sequence Number Description metformin HCl TABLET 850 MG ORAL
    HIC3 C4L
    HIC3 Description ANTIHYPERGLYCEMIC, BIGUANIDE TYPE
    GCN 10811
    HICL Sequence Number 004763
    HICL Sequence Number Description METFORMIN HCL
    Brand/Generic Generic
    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 850
    Active Ingredient Units mg/1
    Substance Name METFORMIN HYDROCHLORIDE
    Labeler Name Aurobindo Pharma Limited
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077095
    Listing Certified Through 2025-12-31

    Package

    NDC 65862-0009-33 (65862000933)

    NDC Package Code 65862-009-33
    Billing NDC 65862000933
    Package 300 TABLET, FILM COATED in 1 BOTTLE (65862-009-33)
    Marketing Start Date 2005-01-14
    NDC Exclude Flag N
    Pricing Information N/A