Search by Drug Name or NDC

    NDC 71335-0618-01 Glipizide 10 mg/1 Details

    Glipizide 10 mg/1

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

    Product Information

    NDC 71335-0618
    Product ID 71335-0618_fc64c052-ae97-1fd5-e053-6394a90ae496
    Associated GPIs 27200030000310
    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
    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 ANDA075795
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-0618-01 (71335061801)

    NDC Package Code 71335-0618-1
    Billing NDC 71335061801
    Package 60 TABLET in 1 BOTTLE (71335-0618-1)
    Marketing Start Date 2005-09-09
    NDC Exclude Flag N
    Pricing Information N/A