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    NDC 00363-0783-24 Fexofenadine hydrochloride 60 mg/1 Details

    Fexofenadine hydrochloride 60 mg/1

    Fexofenadine hydrochloride is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreens Company. The primary component is FEXOFENADINE HYDROCHLORIDE.

    Product Information

    NDC 00363-0783
    Product ID 0363-0783_90bff7b8-9a61-b05c-2408-c08b1eb50c66
    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 Fexofenadine hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Fexofenadine hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 60
    Active Ingredient Units mg/1
    Substance Name FEXOFENADINE HYDROCHLORIDE
    Labeler Name Walgreens Company
    Pharmaceutical Class Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076502
    Listing Certified Through 2024-12-31

    Package

    NDC 00363-0783-24 (00363078324)

    NDC Package Code 0363-0783-24
    Billing NDC 00363078324
    Package 4 BLISTER PACK in 1 CARTON (0363-0783-24) / 6 TABLET in 1 BLISTER PACK
    Marketing Start Date 2020-12-14
    NDC Exclude Flag N
    Pricing Information N/A