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    NDC 71335-0483-01 Fexofenadine hydrochloride 180 mg/1 Details

    Fexofenadine hydrochloride 180 mg/1

    Fexofenadine hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is FEXOFENADINE HYDROCHLORIDE.

    Product Information

    NDC 71335-0483
    Product ID 71335-0483_0d3ec8c9-4703-488b-98c9-1b0935275d78
    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 hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Fexofenadine hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 180
    Active Ingredient Units mg/1
    Substance Name FEXOFENADINE HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202039
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-0483-01 (71335048301)

    NDC Package Code 71335-0483-1
    Billing NDC 71335048301
    Package 30 TABLET, FILM COATED in 1 BOTTLE (71335-0483-1)
    Marketing Start Date 2017-01-25
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 6a401b63-1d8d-46ec-933a-3d6bc8957170 Details

    Revised: 1/2020