Search by Drug Name or NDC

    NDC 50090-5187-00 Tadalafil 20 mg/1 Details

    Tadalafil 20 mg/1

    Tadalafil is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is TADALAFIL.

    Product Information

    NDC 50090-5187
    Product ID 50090-5187_0f676701-853c-43ae-b9a5-9c343eebd825
    Associated GPIs
    GCN Sequence Number 051657
    GCN Sequence Number Description tadalafil TABLET 20 MG ORAL
    HIC3 F2A
    HIC3 Description DRUGS TO TREAT ERECTILE DYSFUNCTION (ED)
    GCN 18996
    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 20
    Active Ingredient Units mg/1
    Substance Name TADALAFIL
    Labeler Name A-S Medication Solutions
    Pharmaceutical Class Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA209539
    Listing Certified Through 2024-12-31

    Package

    NDC 50090-5187-00 (50090518700)

    NDC Package Code 50090-5187-0
    Billing NDC 50090518700
    Package 30 TABLET, FILM COATED in 1 BOTTLE (50090-5187-0)
    Marketing Start Date 2020-09-29
    NDC Exclude Flag N
    Pricing Information N/A