Active Ingredient: NABUMETONE
Proprietary Name: NABUMETONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A079093
Product Number: 001
Approval Date: Feb 27, 2009
Applicant Holder Full Name: OXFORD PHARMACEUTICALS LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information