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    NDC 71205-0220-50 Sildenafil 100 mg/1 Details

    Sildenafil 100 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 71205-0220
    Product ID 71205-220_5d593e03-b6f0-41d0-b7b2-e53d2421a903
    Associated GPIs 40304070100330
    GCN Sequence Number 039191
    GCN Sequence Number Description sildenafil citrate TABLET 100 MG ORAL
    HIC3 F2A
    HIC3 Description DRUGS TO TREAT ERECTILE DYSFUNCTION (ED)
    GCN 57903
    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 100
    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 ANDA203962
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0220-50 (71205022050)

    NDC Package Code 71205-220-50
    Billing NDC 71205022050
    Package 50 TABLET, FILM COATED in 1 BOTTLE (71205-220-50)
    Marketing Start Date 2019-02-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 61c3866e-401d-48b3-a0d2-1e24a33ab512 Details