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    NDC 52083-0239-01 TUSICOF 20; 400; 10 mg/5mL; mg/5mL; mg/5mL Details

    TUSICOF 20; 400; 10 mg/5mL; mg/5mL; mg/5mL

    TUSICOF is a ORAL SYRUP in the HUMAN OTC DRUG category. It is labeled and distributed by Kramer Novis. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 52083-0239
    Product ID 52083-239_1043a161-b529-4a8a-99ca-61d57419b7ec
    Associated GPIs 43997303100980 43997303100315
    GCN Sequence Number 066799
    GCN Sequence Number Description guaifen/dextromethorphan/PE LIQUID 400-20-10 ORAL
    HIC3 B4R
    HIC3 Description NON-OPIOID ANTITUSSIVE-DECONGESTANT-EXPECTORANT
    GCN 29196
    HICL Sequence Number 000216
    HICL Sequence Number Description GUAIFENESIN/DEXTROMETHORPHAN HBR/PHENYLEPHRINE
    Brand/Generic Brand
    Proprietary Name TUSICOF
    Proprietary Name Suffix n/a
    Non-Proprietary Name dextromethorphan, guaifenesin, and phenylephrine
    Product Type HUMAN OTC DRUG
    Dosage Form SYRUP
    Route ORAL
    Active Ingredient Strength 20; 400; 10
    Active Ingredient Units mg/5mL; mg/5mL; mg/5mL
    Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name Kramer Novis
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 52083-0239-01 (52083023901)

    NDC Package Code 52083-239-01
    Billing NDC 52083023901
    Package 30 mL in 1 BOTTLE (52083-239-01)
    Marketing Start Date 2010-08-17
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL e966b75c-4bb4-4216-8247-baada8f5d759 Details

    Revised: 11/2019