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    NDC 71335-0180-01 Glimepiride 4 mg/1 Details

    Glimepiride 4 mg/1

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

    Product Information

    NDC 71335-0180
    Product ID 71335-0180_188733f7-e72a-4217-a2d8-a312cccdc7fc
    Associated GPIs 27200027000340
    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 Glimepiride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Glimepiride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 4
    Active Ingredient Units mg/1
    Substance Name GLIMEPIRIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078181
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-0180-01 (71335018001)

    NDC Package Code 71335-0180-1
    Billing NDC 71335018001
    Package 30 TABLET in 1 BOTTLE (71335-0180-1)
    Marketing Start Date 2014-12-19
    NDC Exclude Flag N
    Pricing Information N/A