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    NDC 71335-1042-02 Glipizide 2.5 mg/1 Details

    Glipizide 2.5 mg/1

    Glipizide is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is GLIPIZIDE.

    Product Information

    NDC 71335-1042
    Product ID 71335-1042_26e6e8e4-da36-4f23-baf1-ab9b2d154bb8
    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 Glipizide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Glipizide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 2.5
    Active Ingredient Units mg/1
    Substance Name GLIPIZIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204720
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-1042-02 (71335104202)

    NDC Package Code 71335-1042-2
    Billing NDC 71335104202
    Package 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1042-2)
    Marketing Start Date 2019-01-08
    NDC Exclude Flag N
    Pricing Information N/A