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    NDC 71335-0150-02 GLYBURIDE 5 mg/1 Details

    GLYBURIDE 5 mg/1

    GLYBURIDE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is GLYBURIDE.

    Product Information

    NDC 71335-0150
    Product ID 71335-0150_fc6435fa-6962-1d3c-e053-6394a90a4e63
    Associated GPIs 27200040000315
    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
    Proprietary Name Suffix n/a
    Non-Proprietary Name GLYBURIDE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name GLYBURIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090937
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-0150-02 (71335015002)

    NDC Package Code 71335-0150-2
    Billing NDC 71335015002
    Package 120 TABLET in 1 BOTTLE (71335-0150-2)
    Marketing Start Date 2022-02-09
    NDC Exclude Flag N
    Pricing Information N/A