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    NDC 69543-0125-50 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 Virtus Pharmaceuticals. The primary component is GLIMEPIRIDE.

    Product Information

    NDC 69543-0125
    Product ID 69543-125_d8f2bca6-5e18-4a1f-b782-9b6e7ba83bc3
    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 Virtus Pharmaceuticals
    Pharmaceutical Class Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202112
    Listing Certified Through 2024-12-31

    Package

    NDC 69543-0125-50 (69543012550)

    NDC Package Code 69543-125-50
    Billing NDC 69543012550
    Package 500 TABLET in 1 BOTTLE (69543-125-50)
    Marketing Start Date 2015-07-14
    NDC Exclude Flag N
    Pricing Information
    Price Per Unit 0.04497
    Pricing Unit EA
    Effective Date 2022-11-23
    NDC Description GLIMEPIRIDE 4 MG TABLET
    Pharmacy Type Indicator C/I
    OTC N
    Explanation Code 1
    Classification for Rate Setting G
    As of Date 2022-11-23
    This pricing file, entitled the NADAC (National Average Drug Acquisition Cost) files, provide state Medicaid agencies with covered outpatient drug prices by averaging survey invoice prices from retail community pharmacies across the United States. These pharmacies include independent retail community pharmacies and chain pharmacies. The prices are updated on a weekly and monthly basis

    Standard Product Labeling (SPL)/Prescribing Information SPL 4419ca50-539c-47e8-ab00-dbb45c7c1814 Details

    Revised: 3/2019