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    NDC 11673-0833-20 Mucus Relief DM Extended Release 30; 600 mg/1; mg/1 Details

    Mucus Relief DM Extended Release 30; 600 mg/1; mg/1

    Mucus Relief DM Extended Release is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by TARGET Corporation. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN.

    Product Information

    NDC 11673-0833
    Product ID 11673-833_7f9325ab-5936-4883-b649-9748009f287f
    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 Mucus Relief DM Extended Release
    Proprietary Name Suffix n/a
    Non-Proprietary Name Guaifenesin, Dextromethorphan HBr
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 30; 600
    Active Ingredient Units mg/1; mg/1
    Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
    Labeler Name TARGET Corporation
    Pharmaceutical Class 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], Uncompetitive NMDA Receptor Ant
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA209692
    Listing Certified Through n/a

    Package

    NDC 11673-0833-20 (11673083320)

    NDC Package Code 11673-833-20
    Billing NDC 11673083320
    Package 20 BLISTER PACK in 1 CARTON (11673-833-20) / 1 TABLET in 1 BLISTER PACK
    Marketing Start Date 2019-01-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL e18db792-3f9b-4ae2-b27e-c15c3bf14fef Details

    Revised: 11/2022