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    NDC 11673-0687-27 up and up naproxen sodium pm 25; 220 mg/1; mg/1 Details

    up and up naproxen sodium pm 25; 220 mg/1; mg/1

    up and up naproxen sodium 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 DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM.

    Product Information

    NDC 11673-0687
    Product ID 11673-687_acc73e3b-e73d-4de2-9eb2-f18d32e9d656
    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 up and up naproxen sodium pm
    Proprietary Name Suffix n/a
    Non-Proprietary Name diphenhydramine hydrochloride, naproxen sodium
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 25; 220
    Active Ingredient Units mg/1; mg/1
    Substance Name DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM
    Labeler Name Target Corporation
    Pharmaceutical Class Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA208499
    Listing Certified Through 2024-12-31

    Package

    NDC 11673-0687-27 (11673068727)

    NDC Package Code 11673-687-27
    Billing NDC 11673068727
    Package 1 BOTTLE in 1 CARTON (11673-687-27) / 80 TABLET, FILM COATED in 1 BOTTLE
    Marketing Start Date 2022-01-25
    NDC Exclude Flag N
    Pricing Information N/A