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    NDC 00363-0578-34 wal tussin dm 20; 200 mg/10mL; mg/10mL Details

    wal tussin dm 20; 200 mg/10mL; mg/10mL

    wal tussin dm is a ORAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreen Company. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN.

    Product Information

    NDC 00363-0578
    Product ID 0363-0578_8ac033e0-4b61-4611-adc2-bf03edfd711c
    Associated GPIs 43997002521220
    GCN Sequence Number 016414
    GCN Sequence Number Description guaifenesin/dextromethorphan SYRUP 100-10MG/5 ORAL
    HIC3 B3T
    HIC3 Description NON-OPIOID ANTITUSSIVE AND EXPECTORANT COMBINATION
    GCN 53495
    HICL Sequence Number 000223
    HICL Sequence Number Description GUAIFENESIN/DEXTROMETHORPHAN HBR
    Brand/Generic Generic
    Proprietary Name wal tussin dm
    Proprietary Name Suffix adult cough and chest congestion
    Non-Proprietary Name Dextromethorphan HBr, Guaifenesin
    Product Type HUMAN OTC DRUG
    Dosage Form SOLUTION
    Route ORAL
    Active Ingredient Strength 20; 200
    Active Ingredient Units mg/10mL; mg/10mL
    Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
    Labeler Name Walgreen Company
    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 00363-0578-34 (00363057834)

    NDC Package Code 0363-0578-34
    Billing NDC 00363057834
    Package 1 BOTTLE in 1 CARTON (0363-0578-34) / 237 mL in 1 BOTTLE
    Marketing Start Date 1995-02-23
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL bab98462-4602-4131-acc4-1c480240afbe Details

    Revised: 12/2019