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EUROCOF - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
EUROCOF
Approved
STANDARD
EUROCOF
AM-Europharma Corporation
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
d589b7c879ba01a1
Company
AM-Europharma Corporation
Type
Standard
Approval Details
Approval Id
d589b7c879ba01a1
Drug Approval Philippines Name
EUROCOF
Product Name
EUROCOF
Registration Number
DRP-7121
Brand Name
EUROCOF
Generic Name
GUAIFENESIN/AMMONIUM CHLORIDE/SODIUM CITRATE/CHLORPHENAMINE MALEATE
Dosage Form
Syrup
Dosage Strength
50mg/ 50mg/100mg/1mg per 5mL
Manufacturer
AM-Europharma Corporation
Distributor
Rilem Pharma Inc.
Issuance Date
28 April 2024
Expiry Date
09 August 2029
Pharmacologic Category
EXPECTORANT/ANTIHISTAMINE
Classification
Over-The-Counter (OTC)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
d589b7c879ba01a1
Type
Standard
Back to Philippines FDA Approvals