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    NDC 00067-7917-06 Theraflu 650; 20; 10 mg/1; mg/1; mg/1 Details

    Theraflu 650; 20; 10 mg/1; mg/1; mg/1

    Theraflu is a ORAL POWDER, FOR SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 00067-7917
    Product ID 0067-7917_09859b07-46e5-fda9-e063-6394a90a6810
    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 Theraflu
    Proprietary Name Suffix Daytime Severe Cold and Cough
    Non-Proprietary Name ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE
    Product Type HUMAN OTC DRUG
    Dosage Form POWDER, FOR SOLUTION
    Route ORAL
    Active Ingredient Strength 650; 20; 10
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M012
    Listing Certified Through 2024-12-31

    Package

    NDC 00067-7917-06 (00067791706)

    NDC Package Code 0067-7917-06
    Billing NDC 00067791706
    Package 6 PACKET in 1 CARTON (0067-7917-06) / 1 POWDER, FOR SOLUTION in 1 PACKET
    Marketing Start Date 2012-09-24
    NDC Exclude Flag N
    Pricing Information N/A