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    NDC 51660-0110-86 Guaifenesin and Dextromethorphan HBr 60; 1200 mg/1; mg/1 Details

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

    Guaifenesin and Dextromethorphan HBr 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 51660-0110
    Product ID 51660-110_82aa6314-52a5-47ba-92c4-2340de30423c
    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 Guaifenesin and Dextromethorphan HBr
    Proprietary Name Suffix n/a
    Non-Proprietary Name Guaifenesin and Dextromethorphan HBr
    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 ANDA
    Application Number ANDA214781
    Listing Certified Through 2024-12-31

    Package

    NDC 51660-0110-86 (51660011086)

    NDC Package Code 51660-110-86
    Billing NDC 51660011086
    Package 2 BLISTER PACK in 1 CARTON (51660-110-86) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
    Marketing Start Date 2021-07-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 07b9854d-1ec6-4c8a-983e-96ed1e2de1c2 Details

    Revised: 8/2021