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    NDC 70934-0629-30 Fexofenadine Hydrochloride 180 mg/1 Details

    Fexofenadine Hydrochloride 180 mg/1

    Fexofenadine Hydrochloride is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is FEXOFENADINE HYDROCHLORIDE.

    Product Information

    NDC 70934-0629
    Product ID 70934-629_e7a29027-ae00-3c50-e053-2995a90aba0d
    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 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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    Pharmaceutical Class Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204507
    Listing Certified Through n/a

    Package

    NDC 70934-0629-30 (70934062930)

    NDC Package Code 70934-629-30
    Billing NDC 70934062930
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70934-629-30)
    Marketing Start Date 2022-08-11
    NDC Exclude Flag N
    Pricing Information N/A