Active Ingredient: IBUPROFEN
Proprietary Name: IBUPROFEN
Dosage Form; Route of Administration: SUSPENSION/DROPS; ORAL
Strength: 50MG/1.25ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A214071
Product Number: 001
Approval Date: Jun 9, 2022
Applicant Holder Full Name: STRIDES PHARMA GLOBAL PTE LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information