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    NDC 00093-7909-01 Tiopronin 100 mg/1 Details

    Tiopronin 100 mg/1

    Tiopronin is a ORAL TABLET, SUGAR COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Teva Pharmaceuticals USA, Inc.. The primary component is TIOPRONIN.

    Product Information

    NDC 00093-7909
    Product ID 0093-7909_af883118-9b27-4cab-9a53-9d85c480bb99
    Associated GPIs 56600050000310
    GCN Sequence Number 008328
    GCN Sequence Number Description tiopronin TABLET 100 MG ORAL
    HIC3 R4A
    HIC3 Description KIDNEY STONE AGENTS
    GCN 35830
    HICL Sequence Number 003714
    HICL Sequence Number Description TIOPRONIN
    Brand/Generic Generic
    Proprietary Name Tiopronin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Tiopronin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, SUGAR COATED
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name TIOPRONIN
    Labeler Name Teva Pharmaceuticals USA, Inc.
    Pharmaceutical Class Cystine Disulfide Reduction [MoA], N-substituted Glycines [CS], Reducing and Complexing Thiol [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA214326
    Listing Certified Through 2024-12-31

    Package

    NDC 00093-7909-01 (00093790901)

    NDC Package Code 0093-7909-01
    Billing NDC 00093790901
    Package 100 TABLET, SUGAR COATED in 1 BOTTLE (0093-7909-01)
    Marketing Start Date 2021-05-17
    NDC Exclude Flag N
    Pricing Information N/A