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    NDC 63629-2202-01 Glipizide 10 mg/1 Details

    Glipizide 10 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 63629-2202
    Product ID 63629-2202_aa97649c-c144-4080-b1c1-1ad50f9aea00
    Associated GPIs 27200030007520
    GCN Sequence Number 021839
    GCN Sequence Number Description glipizide TAB ER 24 10 MG ORAL
    HIC3 C4K
    HIC3 Description ANTIHYPERGLYCEMIC, INSULIN-RELEASE STIMULANT TYPE
    GCN 10843
    HICL Sequence Number 000803
    HICL Sequence Number Description GLIPIZIDE
    Brand/Generic Generic
    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 10
    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 ANDA076159
    Listing Certified Through 2023-12-31

    Package

    NDC 63629-2202-01 (63629220201)

    NDC Package Code 63629-2202-1
    Billing NDC 63629220201
    Package 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2202-1)
    Marketing Start Date 2021-05-19
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 487fd620-1fd2-4ddd-b157-7621d1468b24 Details

    Revised: 4/2022