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    NDC 00527-1934-30 Solifenacin Succinate 10 mg/1 Details

    Solifenacin Succinate 10 mg/1

    Solifenacin Succinate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lannett Company, Inc.. The primary component is SOLIFENACIN SUCCINATE.

    Product Information

    NDC 00527-1934
    Product ID 0527-1934_ee4e17cc-e1c9-419e-838d-f21313e021d4
    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 10
    Active Ingredient Units mg/1
    Substance Name SOLIFENACIN SUCCINATE
    Labeler Name Lannett Company, Inc.
    Pharmaceutical Class Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA211622
    Listing Certified Through 2024-12-31

    Package

    NDC 00527-1934-30 (00527193430)

    NDC Package Code 0527-1934-30
    Billing NDC 00527193430
    Package 30 TABLET, FILM COATED in 1 BOTTLE (0527-1934-30)
    Marketing Start Date 2023-06-06
    NDC Exclude Flag N
    Pricing Information N/A