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    NDC 72789-0048-30 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 PD-Rx Pharmaceuticals, Inc.. The primary component is GLIMEPIRIDE.

    Product Information

    NDC 72789-0048
    Product ID 72789-048_f22ce8c0-067c-396f-e053-2a95a90ad11d
    Associated GPIs 27200027000340
    GCN Sequence Number 025181
    GCN Sequence Number Description glimepiride TABLET 4 MG ORAL
    HIC3 C4K
    HIC3 Description ANTIHYPERGLYCEMIC, INSULIN-RELEASE STIMULANT TYPE
    GCN 05833
    HICL Sequence Number 010485
    HICL Sequence Number Description GLIMEPIRIDE
    Brand/Generic Generic
    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 PD-Rx Pharmaceuticals, Inc.
    Pharmaceutical Class Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077911
    Listing Certified Through 2024-12-31

    Package

    NDC 72789-0048-30 (72789004830)

    NDC Package Code 72789-048-30
    Billing NDC 72789004830
    Package 30 TABLET in 1 BOTTLE, PLASTIC (72789-048-30)
    Marketing Start Date 2020-01-12
    NDC Exclude Flag N
    Pricing Information N/A