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    NDC 47335-0010-72 Tadalafil 5 mg/1 Details

    Tadalafil 5 mg/1

    Tadalafil is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is TADALAFIL.

    Product Information

    NDC 47335-0010
    Product ID 47335-010_5f176ab2-0dba-4418-8aee-27a110ed6396
    Associated GPIs 40304080000305
    GCN Sequence Number 053296
    GCN Sequence Number Description tadalafil TABLET 5 MG ORAL
    HIC3 F2A
    HIC3 Description DRUGS TO TREAT ERECTILE DYSFUNCTION (ED)
    GCN 20736
    HICL Sequence Number 024859
    HICL Sequence Number Description TADALAFIL
    Brand/Generic Generic
    Proprietary Name Tadalafil
    Proprietary Name Suffix n/a
    Non-Proprietary Name Tadalafil
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name TADALAFIL
    Labeler Name Sun Pharmaceutical Industries, Inc.
    Pharmaceutical Class Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA208934
    Listing Certified Through 2024-12-31

    Package

    NDC 47335-0010-72 (47335001072)

    NDC Package Code 47335-010-72
    Billing NDC 47335001072
    Package 1 BLISTER PACK in 1 CARTON (47335-010-72) / 15 TABLET, FILM COATED in 1 BLISTER PACK
    Marketing Start Date 2019-03-26
    NDC Exclude Flag N
    Pricing Information N/A