Active Ingredient: RILUZOLE
Proprietary Name: RILUZOLE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A091417
Product Number: 001
Approval Date: Jun 18, 2013
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
