Active Ingredient: NABUMETONE
Proprietary Name: NABUMETONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 750MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A075179
Product Number: 001
Approval Date: Jun 6, 2000
Applicant Holder Full Name: COPLEY PHARMACEUTICAL INC
Marketing Status:
Discontinued
Patent and Exclusivity Information