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    NDC 71205-0267-30 Sildenafil 50 mg/1 Details

    Sildenafil 50 mg/1

    Sildenafil 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 SILDENAFIL CITRATE.

    Product Information

    NDC 71205-0267
    Product ID 71205-267_4224ad27-bb72-4746-86b7-13c648b8223f
    Associated GPIs 40304070100320
    GCN Sequence Number 039190
    GCN Sequence Number Description sildenafil citrate TABLET 50 MG ORAL
    HIC3 F2A
    HIC3 Description DRUGS TO TREAT ERECTILE DYSFUNCTION (ED)
    GCN 57902
    HICL Sequence Number 018084
    HICL Sequence Number Description SILDENAFIL CITRATE
    Brand/Generic Generic
    Proprietary Name Sildenafil
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sildenafil
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/1
    Substance Name SILDENAFIL CITRATE
    Labeler Name Proficient Rx LP
    Pharmaceutical Class Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077342
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0267-30 (71205026730)

    NDC Package Code 71205-267-30
    Billing NDC 71205026730
    Package 30 TABLET, FILM COATED in 1 BOTTLE (71205-267-30)
    Marketing Start Date 2019-05-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 94eb1f59-2a7d-4230-9ae6-69c34d083326 Details

    Revised: 3/2020