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    NDC 71205-0539-30 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 Proficient Rx LP. The primary component is SOLIFENACIN SUCCINATE.

    Product Information

    NDC 71205-0539
    Product ID 71205-539_31fcb983-1e92-4d12-a997-60346b4fff9f
    Associated GPIs 54100055200320
    GCN Sequence Number 057982
    GCN Sequence Number Description solifenacin succinate TABLET 5 MG ORAL
    HIC3 R1I
    HIC3 Description URINARY TRACT ANTISPASMODIC, M(3) SELECTIVE ANTAG.
    GCN 23276
    HICL Sequence Number 026595
    HICL Sequence Number Description SOLIFENACIN SUCCINATE
    Brand/Generic Generic
    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 Proficient Rx LP
    Pharmaceutical Class Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA211657
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0539-30 (71205053930)

    NDC Package Code 71205-539-30
    Billing NDC 71205053930
    Package 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-539-30)
    Marketing Start Date 2021-02-25
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 31fcb983-1e92-4d12-a997-60346b4fff9f Details

    Revised: 2/2021