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    NDC 68788-8095-06 Glimepiride 2 mg/1 Details

    Glimepiride 2 mg/1

    Glimepiride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is GLIMEPIRIDE.

    Product Information

    NDC 68788-8095
    Product ID 68788-8095_0a11a287-52a6-4163-b1f9-6d424d7fcb70
    Associated GPIs 27200027000320
    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 2
    Active Ingredient Units mg/1
    Substance Name GLIMEPIRIDE
    Labeler Name Preferred Pharmaceuticals Inc.
    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 68788-8095-06 (68788809506)

    NDC Package Code 68788-8095-6
    Billing NDC 68788809506
    Package 60 TABLET in 1 BOTTLE (68788-8095-6)
    Marketing Start Date 2021-10-06
    NDC Exclude Flag N
    Pricing Information N/A