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: A090445
Product Number: 001
Approval Date: Jan 12, 2011
Applicant Holder Full Name: ANNORA PHARMA PRIVATE LTD
Marketing Status:
Prescription
Patent and Exclusivity Information