Active Ingredient: IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
Proprietary Name: IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG;30MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077628
Product Number: 001
Approval Date: Aug 14, 2006
Applicant Holder Full Name: STRIDES PHARMA GLOBAL PTE LTD
Marketing Status:
Over-the-counter
Patent and Exclusivity Information
