Active Ingredient: NABUMETONE
Proprietary Name: NABUMETONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 750MG
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A078671
Product Number: 002
Approval Date: Mar 7, 2008
Applicant Holder Full Name: INVAGEN PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information