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    NDC 00363-0702-26 wal tussin dm max 20; 400 mg/10mL; mg/10mL Details

    wal tussin dm max 20; 400 mg/10mL; mg/10mL

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

    Product Information

    NDC 00363-0702
    Product ID 0363-0702_5d27646b-bea0-4472-8b84-1ff0d699ea56
    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 wal tussin dm max
    Proprietary Name Suffix n/a
    Non-Proprietary Name Dextromethorphan HBr, Guaifenesin
    Product Type HUMAN OTC DRUG
    Dosage Form SUSPENSION
    Route ORAL
    Active Ingredient Strength 20; 400
    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 2023-12-31

    Package

    NDC 00363-0702-26 (00363070226)

    NDC Package Code 0363-0702-26
    Billing NDC 00363070226
    Package 1 BOTTLE in 1 CARTON (0363-0702-26) / 118 mL in 1 BOTTLE
    Marketing Start Date 2014-10-31
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 6de75dcf-30c1-4acc-a722-967c91676e4f Details

    Revised: 12/2019