Active Ingredient: KETOPROFEN
Proprietary Name: KETOPROFEN
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074879
Product Number: 001
Approval Date: Dec 10, 1997
Applicant Holder Full Name: ALKERMES GAINESVILLE LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information