Active Ingredient: FENOPROFEN CALCIUM
Proprietary Name: FENOPROFEN CALCIUM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 600MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A072429
Product Number: 001
Approval Date: Aug 17, 1988
Applicant Holder Full Name: STRIDES PHARMA GLOBAL PTE LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information