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    NDC 68788-8066-06 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 Preferred Pharmaceuticals Inc.. The primary component is GLIMEPIRIDE.

    Product Information

    NDC 68788-8066
    Product ID 68788-8066_0b0478bb-f82e-4d9c-8ed7-58a8e7c696f8
    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 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 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 68788-8066-06 (68788806606)

    NDC Package Code 68788-8066-6
    Billing NDC 68788806606
    Package 60 TABLET in 1 BOTTLE (68788-8066-6)
    Marketing Start Date 2021-08-16
    NDC Exclude Flag N
    Pricing Information N/A