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    NDC 50991-0740-01 DECONEX 17.5; 400; 10 mg/1; mg/1; mg/1 Details

    DECONEX 17.5; 400; 10 mg/1; mg/1; mg/1

    DECONEX is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Poly Pharmaceuticals, Inc.. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 50991-0740
    Product ID 50991-740_f17bdf02-2295-daaf-e053-2995a90add07
    Associated GPIs 43997303100345
    GCN Sequence Number 079878
    GCN Sequence Number Description guaifen/dextromethorphan/PE TABLET 400-17.5MG ORAL
    HIC3 B4R
    HIC3 Description NON-OPIOID ANTITUSSIVE-DECONGESTANT-EXPECTORANT
    GCN 46479
    HICL Sequence Number 000216
    HICL Sequence Number Description GUAIFENESIN/DEXTROMETHORPHAN HBR/PHENYLEPHRINE
    Brand/Generic Brand
    Proprietary Name DECONEX
    Proprietary Name Suffix DMX
    Non-Proprietary Name Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 17.5; 400; 10
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name Poly Pharmaceuticals, Inc.
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], 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
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 50991-0740-01 (50991074001)

    NDC Package Code 50991-740-01
    Billing NDC 50991074001
    Package 100 TABLET in 1 BOTTLE (50991-740-01)
    Marketing Start Date 2019-06-01
    NDC Exclude Flag N
    Pricing Information N/A