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    NDC 00031-8750-18 Robitussin Maximum Strength Severe Cough Plus Sore Throat 650; 20 mg/20mL; mg/20mL Details

    Robitussin Maximum Strength Severe Cough Plus Sore Throat 650; 20 mg/20mL; mg/20mL

    Robitussin Maximum Strength Severe Cough Plus Sore Throat is a ORAL LIQUID 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.

    Product Information

    NDC 00031-8750
    Product ID 0031-8750_90199483-457d-4f7b-915d-72250ec14390
    Associated GPIs 43995502200925
    GCN Sequence Number 080839
    GCN Sequence Number Description acetaminophen/dextromethorphan LIQUID 325-10/10 ORAL
    HIC3 B4A
    HIC3 Description NON-OPIOID ANTITUSSIVE-ANALGESIC COMBINATIONS
    GCN 47821
    HICL Sequence Number 006331
    HICL Sequence Number Description ACETAMINOPHEN/DEXTROMETHORPHAN HBR
    Brand/Generic Generic
    Proprietary Name Robitussin Maximum Strength Severe Cough Plus Sore Throat
    Proprietary Name Suffix n/a
    Non-Proprietary Name acetaminophen, dextromethorphan hydrobromide
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 650; 20
    Active Ingredient Units mg/20mL; mg/20mL
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE
    Labeler Name GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
    Pharmaceutical Class Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 00031-8750-18 (00031875018)

    NDC Package Code 0031-8750-18
    Billing NDC 00031875018
    Package 1 BOTTLE in 1 CARTON (0031-8750-18) / 237 mL in 1 BOTTLE
    Marketing Start Date 2017-04-10
    NDC Exclude Flag N
    Pricing Information N/A