Active Ingredient: OXCARBAZEPINE
Proprietary Name: OXCARBAZEPINE
Dosage Form; Route of Administration: SUSPENSION; ORAL
Strength: 300MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A078734
Product Number: 001
Approval Date: Jun 26, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information