Active Ingredient: NABUMETONE
Proprietary Name: NABUMETONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075280
Product Number: 001
Approval Date: Feb 25, 2002
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status:
Prescription
Patent and Exclusivity Information