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    NDC 00067-2039-50 EXCEDRIN 250; 250; 65 mg/1; mg/1; mg/1 Details

    EXCEDRIN 250; 250; 65 mg/1; mg/1; mg/1

    EXCEDRIN 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; ASPIRIN; CAFFEINE.

    Product Information

    NDC 00067-2039
    Product ID 0067-2039_06183414-a911-4a52-8f13-c78e3ec52956
    Associated GPIs 64990003200350
    GCN Sequence Number 040186
    GCN Sequence Number Description aspirin/acetaminophen/caffeine TABLET 250-250-65 ORAL
    HIC3 H3D
    HIC3 Description ANALGESIC/ANTIPYRETICS, SALICYLATES
    GCN 10414
    HICL Sequence Number 001807
    HICL Sequence Number Description ASPIRIN/ACETAMINOPHEN/CAFFEINE
    Brand/Generic Brand
    Proprietary Name EXCEDRIN
    Proprietary Name Suffix MIGRAINE
    Non-Proprietary Name Acetaminophen, Aspirin (NSAID) and Caffeine
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 250; 250; 65
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name ACETAMINOPHEN; ASPIRIN; CAFFEINE
    Labeler Name GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
    Pharmaceutical Class Anti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [E
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA020802
    Listing Certified Through 2024-12-31

    Package

    NDC 00067-2039-50 (00067203950)

    NDC Package Code 0067-2039-50
    Billing NDC 00067203950
    Package 1 BOTTLE in 1 CARTON (0067-2039-50) / 50 TABLET, FILM COATED in 1 BOTTLE
    Marketing Start Date 2010-02-15
    NDC Exclude Flag N
    Pricing Information N/A