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    NDC 63629-2286-01 Ursodiol 250 mg/1 Details

    Ursodiol 250 mg/1

    Ursodiol is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is URSODIOL.

    Product Information

    NDC 63629-2286
    Product ID 63629-2286_15aa5fa7-2054-473e-bd59-b6f228f01cc7
    Associated GPIs 52100040000325
    GCN Sequence Number 024333
    GCN Sequence Number Description ursodiol TABLET 250 MG ORAL
    HIC3 D7A
    HIC3 Description BILE SALTS
    GCN 01072
    HICL Sequence Number 001370
    HICL Sequence Number Description URSODIOL
    Brand/Generic Generic
    Proprietary Name Ursodiol
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ursodiol
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 250
    Active Ingredient Units mg/1
    Substance Name URSODIOL
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Bile Acid [EPC], Bile Acids and Salts [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202540
    Listing Certified Through 2024-12-31

    Package

    NDC 63629-2286-01 (63629228601)

    NDC Package Code 63629-2286-1
    Billing NDC 63629228601
    Package 100 TABLET, FILM COATED in 1 BOTTLE (63629-2286-1)
    Marketing Start Date 2021-03-29
    NDC Exclude Flag N
    Pricing Information N/A