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    NDC 51660-0073-54 Guaifenesin and Dextromethorphan Hydrobromide 60; 1200 mg/1; mg/1 Details

    Guaifenesin and Dextromethorphan Hydrobromide 60; 1200 mg/1; mg/1

    Guaifenesin and Dextromethorphan Hydrobromide is a ORAL TABLET, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by OHM LABORATORIES INC. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN.

    Product Information

    NDC 51660-0073
    Product ID 51660-073_62d9d841-9307-45a7-89a7-cba5cded1462
    Associated GPIs 43997002527475
    GCN Sequence Number 042105
    GCN Sequence Number Description guaifenesin/dextromethorphan TAB ER 12H 1200-60MG ORAL
    HIC3 B3T
    HIC3 Description NON-OPIOID ANTITUSSIVE AND EXPECTORANT COMBINATION
    GCN 93677
    HICL Sequence Number 000223
    HICL Sequence Number Description GUAIFENESIN/DEXTROMETHORPHAN HBR
    Brand/Generic Generic
    Proprietary Name Guaifenesin and Dextromethorphan Hydrobromide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Guaifenesin and Dextromethorphan Hydrobromide
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 60; 1200
    Active Ingredient Units mg/1; mg/1
    Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
    Labeler Name OHM LABORATORIES 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 NDA
    Application Number NDA021620
    Listing Certified Through 2022-12-31

    Package

    NDC 51660-0073-54 (51660007354)

    NDC Package Code 51660-073-54
    Billing NDC 51660007354
    Package 1 BLISTER PACK in 1 CARTON (51660-073-54) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
    Marketing Start Date 2017-12-10
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL ed496cde-4355-45c4-80f0-84df06c32523 Details

    Revised: 10/2018