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    NDC 68788-8138-08 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 Preferred Pharmaceuticals Inc... The primary component is GLIPIZIDE.

    Product Information

    NDC 68788-8138
    Product ID 68788-8138_9e4ae4bc-580d-4dde-9b32-3ca7d472cdca
    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 Preferred Pharmaceuticals Inc..
    Pharmaceutical Class Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA074223
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-8138-08 (68788813808)

    NDC Package Code 68788-8138-8
    Billing NDC 68788813808
    Package 180 TABLET in 1 BOTTLE, PLASTIC (68788-8138-8)
    Marketing Start Date 2022-02-11
    NDC Exclude Flag N
    Pricing Information N/A