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    NDC 67877-0648-11 Sildenafil Citrate 10 mg/mL Details

    Sildenafil Citrate 10 mg/mL

    Sildenafil Citrate is a ORAL POWDER, FOR SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Ascend Laboratories, LLC. The primary component is SILDENAFIL CITRATE.

    Product Information

    NDC 67877-0648
    Product ID 67877-648_a85cb8be-4aea-410c-a921-15d44a6ff48a
    Associated GPIs
    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 Citrate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sildenafil Citrate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form POWDER, FOR SUSPENSION
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/mL
    Substance Name SILDENAFIL CITRATE
    Labeler Name Ascend Laboratories, LLC
    Pharmaceutical Class Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA212440
    Listing Certified Through 2024-12-31

    Package

    NDC 67877-0648-11 (67877064811)

    NDC Package Code 67877-648-11
    Billing NDC 67877064811
    Package 1 BOTTLE, GLASS in 1 CARTON (67877-648-11) / 112 mL in 1 BOTTLE, GLASS
    Marketing Start Date 2019-11-29
    NDC Exclude Flag N
    Pricing Information N/A