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    NDC 76281-0504-24 TUSSIN CF 10; 100; 5 mg/5mL; mg/5mL; mg/5mL Details

    TUSSIN CF 10; 100; 5 mg/5mL; mg/5mL; mg/5mL

    TUSSIN CF is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by AptaPharma Inc.. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 76281-0504
    Product ID 76281-504_9560bce8-d705-4882-87cf-fde3c283513f
    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 CF
    Proprietary Name Suffix n/a
    Non-Proprietary Name DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 10; 100; 5
    Active Ingredient Units mg/5mL; mg/5mL; mg/5mL
    Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name AptaPharma 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 DRUG
    Application Number M012
    Listing Certified Through 2024-12-31

    Package

    NDC 76281-0504-24 (76281050424)

    NDC Package Code 76281-504-24
    Billing NDC 76281050424
    Package 118 mL in 1 BOTTLE (76281-504-24)
    Marketing Start Date 2020-09-30
    NDC Exclude Flag N
    Pricing Information N/A