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    NDC 47335-0236-64 ambrisentan 5 mg/1 Details

    ambrisentan 5 mg/1

    ambrisentan is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is AMBRISENTAN.

    Product Information

    NDC 47335-0236
    Product ID 47335-236_884d2d52-fa1a-4895-823c-e62916bffefe
    Associated GPIs 40160007000310
    GCN Sequence Number 062792
    GCN Sequence Number Description ambrisentan TABLET 5 MG ORAL
    HIC3 B1B
    HIC3 Description PULMONARY ANTI-HTN, ENDOTHELIN RECEPTOR ANTAGONIST
    GCN 98566
    HICL Sequence Number 034849
    HICL Sequence Number Description AMBRISENTAN
    Brand/Generic Generic
    Proprietary Name ambrisentan
    Proprietary Name Suffix n/a
    Non-Proprietary Name ambrisentan
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name AMBRISENTAN
    Labeler Name Sun Pharmaceutical Industries, Inc.
    Pharmaceutical Class Endothelin Receptor Antagonist [EPC], Endothelin Receptor Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA210784
    Listing Certified Through 2024-12-31

    Package

    NDC 47335-0236-64 (47335023664)

    NDC Package Code 47335-236-64
    Billing NDC 47335023664
    Package 3 BLISTER PACK in 1 CARTON (47335-236-64) / 10 TABLET, FILM COATED in 1 BLISTER PACK (47335-236-60)
    Marketing Start Date 2019-04-29
    NDC Exclude Flag N
    Pricing Information N/A