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    NDC 00363-0844-80 All Night Pain Relief PM 25; 220 mg/1; mg/1 Details

    All Night Pain Relief PM 25; 220 mg/1; mg/1

    All Night Pain Relief PM is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreens. The primary component is DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM.

    Product Information

    NDC 00363-0844
    Product ID 0363-0844_022bd9fe-6d43-4ca8-8dd8-4ecb2c198a85
    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 All Night Pain Relief PM
    Proprietary Name Suffix n/a
    Non-Proprietary Name Naproxen Sodium
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 25; 220
    Active Ingredient Units mg/1; mg/1
    Substance Name DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM
    Labeler Name Walgreens
    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 ANDA209726
    Listing Certified Through 2024-12-31

    Package

    NDC 00363-0844-80 (00363084480)

    NDC Package Code 0363-0844-80
    Billing NDC 00363084480
    Package 80 TABLET in 1 BOTTLE, PLASTIC (0363-0844-80)
    Marketing Start Date 2018-12-31
    NDC Exclude Flag N
    Pricing Information N/A