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    NDC 11673-0437-78 up and up acetaminophen pm 500; 25 mg/1; mg/1 Details

    up and up acetaminophen pm 500; 25 mg/1; mg/1

    up and up acetaminophen pm is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Target Corporation. The primary component is ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE.

    Product Information

    NDC 11673-0437
    Product ID 11673-437_61f22a5a-85d6-4b69-9d08-6d97a6a2b07c
    Associated GPIs
    GCN Sequence Number 003699
    GCN Sequence Number Description acetaminophen/diphenhydramine TABLET 500MG-25MG ORAL
    HIC3 B5S
    HIC3 Description ANALGESIC, NON-SAL.- 1ST GENERATION ANTIHISTAMINE
    GCN 70221
    HICL Sequence Number 001861
    HICL Sequence Number Description ACETAMINOPHEN/DIPHENHYDRAMINE HCL
    Brand/Generic Generic
    Proprietary Name up and up acetaminophen pm
    Proprietary Name Suffix extra strength
    Non-Proprietary Name Acetaminophen, 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 Target Corporation
    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 11673-0437-78 (11673043778)

    NDC Package Code 11673-437-78
    Billing NDC 11673043778
    Package 1 BOTTLE in 1 CARTON (11673-437-78) / 100 TABLET, FILM COATED in 1 BOTTLE
    Marketing Start Date 2009-07-10
    NDC Exclude Flag N
    Pricing Information N/A