Last update 08 Nov 2025

Acetaminophen/Chlorpheniramine Maleate/Methylephedrine Hydrochloride/Pseudoephedrine Hydrochloride/Dextromethorphan Hydrobromide Hydrate/Guaifenesin

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms
윈콜드연질캡슐
Target
H1 receptor x σ1 receptor
Action
antagonists, agonists
Mechanism
H1 receptor antagonists(Histamine H1 receptor antagonists), σ1 receptor agonists(Sigma opioid receptor agonists)
Therapeutic Areas
Infectious DiseasesRespiratory Diseases
Active Indication
Common Cold
Inactive Indication-
Originator Organization
CMG Pharmaceutical Co., Ltd.CMG Pharmaceutical Co., Ltd.
Active Organization
CMG Pharmaceutical Co., Ltd.CMG Pharmaceutical Co., Ltd.
Inactive Organization-
License Organization-
Drug Highest PhaseApproved
First Approval Date
South Korea (08 Oct 2024),
Common Cold
Regulation-
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Structure/Sequence

Molecular FormulaC10H16ClNO
InChIKeyBALXUFOVQVENIU-KXNXZCPBSA-N
CAS Registry345-78-8
View All Structures (9)

Related

100 Clinical Results associated with Acetaminophen/Chlorpheniramine Maleate/Methylephedrine Hydrochloride/Pseudoephedrine Hydrochloride/Dextromethorphan Hydrobromide Hydrate/Guaifenesin
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100 Translational Medicine associated with Acetaminophen/Chlorpheniramine Maleate/Methylephedrine Hydrochloride/Pseudoephedrine Hydrochloride/Dextromethorphan Hydrobromide Hydrate/Guaifenesin
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100 Patents (Medical) associated with Acetaminophen/Chlorpheniramine Maleate/Methylephedrine Hydrochloride/Pseudoephedrine Hydrochloride/Dextromethorphan Hydrobromide Hydrate/Guaifenesin
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100 Deals associated with Acetaminophen/Chlorpheniramine Maleate/Methylephedrine Hydrochloride/Pseudoephedrine Hydrochloride/Dextromethorphan Hydrobromide Hydrate/Guaifenesin
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R&D Status

10 top approved records.
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IndicationCountry/LocationOrganizationDate
Common Cold
South Korea
CMG Pharmaceutical Co., Ltd.CMG Pharmaceutical Co., Ltd.
08 Oct 2024
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

No Data

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Deal

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Core Patent

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Clinical Trial

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Approval

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Regulation

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