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    NDC 70954-0433-10 Tadalafil 5 mg/1 Details

    Tadalafil 5 mg/1

    Tadalafil is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by ANI Pharmaceuticals, Inc.. The primary component is TADALAFIL.

    Product Information

    NDC 70954-0433
    Product ID 70954-433_1dace1e7-c617-492f-bb0d-141bf4e673db
    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 Tadalafil
    Proprietary Name Suffix n/a
    Non-Proprietary Name Tadalafil
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name TADALAFIL
    Labeler Name ANI Pharmaceuticals, Inc.
    Pharmaceutical Class Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA215949
    Listing Certified Through 2024-12-31

    Package

    NDC 70954-0433-10 (70954043310)

    NDC Package Code 70954-433-10
    Billing NDC 70954043310
    Package 30 TABLET in 1 BOTTLE (70954-433-10)
    Marketing Start Date 2023-03-06
    NDC Exclude Flag N
    Pricing Information N/A