Search by Drug Name or NDC

    NDC 68788-7974-06 Sildenafil 20 mg/1 Details

    Sildenafil 20 mg/1

    Sildenafil is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is SILDENAFIL CITRATE.

    Product Information

    NDC 68788-7974
    Product ID 68788-7974_e30a4fd2-902e-48e7-8b2f-bd07ac046e16
    Associated GPIs 40143060100320
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Sildenafil
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sildenafil
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name SILDENAFIL CITRATE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA210394
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7974-06 (68788797406)

    NDC Package Code 68788-7974-6
    Billing NDC 68788797406
    Package 60 TABLET in 1 BOTTLE (68788-7974-6)
    Marketing Start Date 2021-07-28
    NDC Exclude Flag N
    Pricing Information N/A