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    NDC 50269-0226-54 Benadryl Ultra Tab 25 mg/1 Details

    Benadryl Ultra Tab 25 mg/1

    Benadryl Ultra Tab is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by JC World Bell Wholesale Co., Inc.. The primary component is DIPHENHYDRAMINE HYDROCHLORIDE.

    Product Information

    NDC 50269-0226
    Product ID 50269-226_09738b82-8e10-7e4c-e063-6294a90a4dd0
    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 Benadryl Ultra Tab
    Proprietary Name Suffix n/a
    Non-Proprietary Name DIPHENHYDRAMINE HYDROCHLORIDE
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 25
    Active Ingredient Units mg/1
    Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
    Labeler Name JC World Bell Wholesale Co., Inc.
    Pharmaceutical Class Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M012
    Listing Certified Through 2024-12-31

    Package

    NDC 50269-0226-54 (50269022654)

    NDC Package Code 50269-226-54
    Billing NDC 50269022654
    Package 25 TABLET, FILM COATED in 1 BOX (50269-226-54)
    Marketing Start Date 2018-08-16
    NDC Exclude Flag N
    Pricing Information N/A