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    NDC 37808-0359-34 Tussin DM 20; 200 mg/10mL; mg/10mL Details

    Tussin DM 20; 200 mg/10mL; mg/10mL

    Tussin DM is a ORAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by H E B. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN.

    Product Information

    NDC 37808-0359
    Product ID 37808-359_d1da766f-79d9-4fd6-a228-757aea65465d
    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 Tussin DM
    Proprietary Name Suffix n/a
    Non-Proprietary Name Dextromethorphan Hydrobromide, 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 H E B
    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 37808-0359-34 (37808035934)

    NDC Package Code 37808-359-34
    Billing NDC 37808035934
    Package 1 BOTTLE in 1 CARTON (37808-359-34) / 237 mL in 1 BOTTLE
    Marketing Start Date 1991-08-09
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL eff701cb-30b2-40de-8c87-b52d5d22fa01 Details

    Revised: 5/2018