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    NDC 65862-0690-05 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 Aurobindo Pharma Limited. The primary component is SILDENAFIL CITRATE.

    Product Information

    NDC 65862-0690
    Product ID 65862-690_f3ce5e4b-0b8b-4db0-b3b9-761691f32729
    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 Aurobindo Pharma Limited
    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 65862-0690-05 (65862069005)

    NDC Package Code 65862-690-05
    Billing NDC 65862069005
    Package 500 TABLET, FILM COATED in 1 BOTTLE (65862-690-05)
    Marketing Start Date 2023-07-10
    NDC Exclude Flag N
    Pricing Information N/A