Search by Drug Name or NDC

    NDC 71335-1088-09 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 Bryant Ranch Prepack. The primary component is SILDENAFIL CITRATE.

    Product Information

    NDC 71335-1088
    Product ID 71335-1088_4188c3f7-e2f5-4134-8af6-c78a64427e29
    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 Bryant Ranch Prepack
    Pharmaceutical Class Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202659
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-1088-09 (71335108809)

    NDC Package Code 71335-1088-9
    Billing NDC 71335108809
    Package 60 TABLET, FILM COATED in 1 BOTTLE (71335-1088-9)
    Marketing Start Date 2022-02-09
    NDC Exclude Flag N
    Pricing Information N/A