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    NDC 71335-0179-05 Glyburide and Metformin Hydrochloride 2.5; 500 mg/1; mg/1 Details

    Glyburide and Metformin Hydrochloride 2.5; 500 mg/1; mg/1

    Glyburide and Metformin Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is GLYBURIDE; METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 71335-0179
    Product ID 71335-0179_2f71afe5-b072-4ff2-a6fb-76894a8f6335
    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 Glyburide and Metformin Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Glyburide and Metformin Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 2.5; 500
    Active Ingredient Units mg/1; mg/1
    Substance Name GLYBURIDE; METFORMIN HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS], Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077870
    Listing Certified Through 2023-12-31

    Package

    NDC 71335-0179-05 (71335017905)

    NDC Package Code 71335-0179-5
    Billing NDC 71335017905
    Package 180 TABLET, FILM COATED in 1 BOTTLE (71335-0179-5)
    Marketing Start Date 2021-12-27
    NDC Exclude Flag N
    Pricing Information N/A