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    NDC 71335-1729-02 Solifenacin Succinate 5 mg/1 Details

    Solifenacin Succinate 5 mg/1

    Solifenacin Succinate 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 SOLIFENACIN SUCCINATE.

    Product Information

    NDC 71335-1729
    Product ID 71335-1729_507a97b3-b3e4-427f-8d23-205653db2b17
    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 Solifenacin Succinate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Solifenacin Succinate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name SOLIFENACIN SUCCINATE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA210224
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-1729-02 (71335172902)

    NDC Package Code 71335-1729-2
    Billing NDC 71335172902
    Package 90 TABLET, FILM COATED in 1 BOTTLE (71335-1729-2)
    Marketing Start Date 2021-12-29
    NDC Exclude Flag N
    Pricing Information N/A