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    NDC 68788-7856-01 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 Preferred Pharmaceuticals Inc.. The primary component is GLIPIZIDE.

    Product Information

    NDC 68788-7856
    Product ID 68788-7856_535183dc-255d-41d6-a4a9-305fb5f1d55a
    Associated GPIs 27200030007520
    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 10
    Active Ingredient Units mg/1
    Substance Name GLIPIZIDE
    Labeler Name Preferred Pharmaceuticals Inc.
    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 68788-7856-01 (68788785601)

    NDC Package Code 68788-7856-1
    Billing NDC 68788785601
    Package 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7856-1)
    Marketing Start Date 2021-01-29
    NDC Exclude Flag N
    Pricing Information N/A