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    NDC 70518-1063-01 Glipizide 5 mg/1 Details

    Glipizide 5 mg/1

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

    Product Information

    NDC 70518-1063
    Product ID 70518-1063_02a68654-f6ec-c351-e063-6294a90a94c2
    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 5
    Active Ingredient Units mg/1
    Substance Name GLIPIZIDE
    Labeler Name REMEDYREPACK 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 70518-1063-01 (70518106301)

    NDC Package Code 70518-1063-1
    Billing NDC 70518106301
    Package 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1063-1)
    Marketing Start Date 2018-03-21
    NDC Exclude Flag N
    Pricing Information N/A