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    NDC 00135-0608-02 PANADOL 500; 25 mg/1; mg/1 Details

    PANADOL 500; 25 mg/1; mg/1

    PANADOL is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE.

    Product Information

    NDC 00135-0608
    Product ID 0135-0608_b26b54e1-fce0-4e33-9323-6360ff62963e
    Associated GPIs 60309902200310
    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 PANADOL
    Proprietary Name Suffix PM
    Non-Proprietary Name acetaminophen and diphenhydramine HCl
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 500; 25
    Active Ingredient Units mg/1; mg/1
    Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
    Labeler Name GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
    Pharmaceutical Class Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH NOT FINAL
    Application Number part343
    Listing Certified Through 2024-12-31

    Package

    NDC 00135-0608-02 (00135060802)

    NDC Package Code 0135-0608-02
    Billing NDC 00135060802
    Package 1 BOTTLE in 1 CARTON (0135-0608-02) / 50 TABLET, FILM COATED in 1 BOTTLE
    Marketing Start Date 2016-12-01
    NDC Exclude Flag N
    Pricing Information N/A