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    NDC 76281-0310-26 Tussin DM 20; 200 mg/10mL; mg/10mL Details

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

    Tussin DM 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.

    Product Information

    NDC 76281-0310
    Product ID 76281-310_46ce9f7c-cc2d-4ad2-aba3-04c373ea18cc
    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 HBr, GUAIFENESIN
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 20; 200
    Active Ingredient Units mg/10mL; mg/10mL
    Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
    Labeler Name AptaPharma Inc.
    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 2022-12-31

    Package

    NDC 76281-0310-26 (76281031026)

    NDC Package Code 76281-310-26
    Billing NDC 76281031026
    Package 237 mL in 1 BOTTLE (76281-310-26)
    Marketing Start Date 2018-08-01
    NDC Exclude Flag N
    Pricing Information N/A
    << 76281-0309-26 76281-0311-26 >>

    Contents

    Standard Product Labeling (SPL)/Prescribing Information SPL 7eead561-ee36-4d85-936b-f472c56a75c6 Details

    Revised: 12/2019
    Document Id: 46ce9f7c-cc2d-4ad2-aba3-04c373ea18cc
    Set id: 7eead561-ee36-4d85-936b-f472c56a75c6
    Version: 2
    Effective Time: 20191209