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    NDC 70518-1513-00 GLYBURIDE 2.5 mg/1 Details

    GLYBURIDE 2.5 mg/1

    GLYBURIDE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is GLYBURIDE.

    Product Information

    NDC 70518-1513
    Product ID 70518-1513_f9db84af-79aa-b444-e053-6294a90a001e
    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 GLYBURIDE
    Proprietary Name Suffix n/a
    Non-Proprietary Name GLYBURIDE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 2.5
    Active Ingredient Units mg/1
    Substance Name GLYBURIDE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090937
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-1513-00 (70518151300)

    NDC Package Code 70518-1513-0
    Billing NDC 70518151300
    Package 30 TABLET in 1 BLISTER PACK (70518-1513-0)
    Marketing Start Date 2018-10-10
    NDC Exclude Flag N
    Pricing Information N/A