Last update 03 Dec 2024

Acetaminophen/Pseudoephedrine Hydrochloride/Dextromethorphan Hydrobromide Hydrate/Chlorpheniramine Maleate

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms
恺诺, 氨麻美敏, 酚麻美敏
+ [1]
Target
COX x H1 receptor x NMDA receptor x α-adrenergic receptor x σ1 receptor
Mechanism
COX inhibitors(Cyclooxygenases inhibitors), H1 receptor modulators(Histamine H1 receptor modulators), NMDA receptor antagonists(Glutamate [NMDA] receptor antagonists)
Therapeutic Areas
Infectious DiseasesRespiratory Diseases
Active Indication
Common ColdInfluenza, Human
Inactive Indication-
Originator Organization
Yangtze River Pharmaceutical Co. Ltd.Yangtze River Pharmaceutical Co. Ltd.
Active Organization
JW PHARMACEUTICAL Corp.JW PHARMACEUTICAL Corp.Sino-American Shanghai Squibb Pharmaceuticals Ltd.Sino-American Shanghai Squibb Pharmaceuticals Ltd.
Inactive Organization-
Drug Highest PhaseApproved
First Approval Date
CN (01 Jan 1997),
Influenza, Human
Regulation-
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Structure

Molecular FormulaC10H16ClNO
InChIKeyBALXUFOVQVENIU-KXNXZCPBSA-N
CAS Registry345-78-8
View All Structures (4)

Related

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

10 top approved records.
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IndicationCountry/LocationOrganizationDate
Common Cold
KR
JW PHARMACEUTICAL Corp.JW PHARMACEUTICAL Corp.
21 Nov 2024
Influenza, Human
CN
Sino-American Shanghai Squibb Pharmaceuticals Ltd.Sino-American Shanghai Squibb Pharmaceuticals Ltd.
01 Jan 1997
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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Approval

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Regulation

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