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    NDC 68788-7449-03 Fexofenadine HCL 180 mg/1 Details

    Fexofenadine HCL 180 mg/1

    Fexofenadine HCL is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is FEXOFENADINE HYDROCHLORIDE.

    Product Information

    NDC 68788-7449
    Product ID 68788-7449_74ac42b3-65d0-4c78-af04-75b8990ac95b
    Associated GPIs 41550024100350
    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 Fexofenadine HCL
    Proprietary Name Suffix n/a
    Non-Proprietary Name Fexofenadine HCL
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 180
    Active Ingredient Units mg/1
    Substance Name FEXOFENADINE HYDROCHLORIDE
    Labeler Name Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204097
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7449-03 (68788744903)

    NDC Package Code 68788-7449-3
    Billing NDC 68788744903
    Package 30 TABLET in 1 BOTTLE (68788-7449-3)
    Marketing Start Date 2019-12-27
    NDC Exclude Flag N
    Pricing Information N/A