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    NDC 68788-8142-01 Tussin Multi Symptom Cold CF 20; 200; 10 mg/10mL; mg/10mL; mg/10mL Details

    Tussin Multi Symptom Cold CF 20; 200; 10 mg/10mL; mg/10mL; mg/10mL

    Tussin Multi Symptom Cold CF is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 68788-8142
    Product ID 68788-8142_40e7b36f-b258-4381-96d1-9d7176c43df9
    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 Multi Symptom Cold CF
    Proprietary Name Suffix Adult
    Non-Proprietary Name Dextromethorphan HBr, Guaifenesin, Phenylephrine
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 20; 200; 10
    Active Ingredient Units mg/10mL; mg/10mL; mg/10mL
    Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-8142-01 (68788814201)

    NDC Package Code 68788-8142-1
    Billing NDC 68788814201
    Package 1 BOTTLE, PLASTIC in 1 BOX (68788-8142-1) / 118 mL in 1 BOTTLE, PLASTIC
    Marketing Start Date 2022-09-01
    NDC Exclude Flag N
    Pricing Information N/A