Active Ingredient: NARATRIPTAN HYDROCHLORIDE
Proprietary Name: NARATRIPTAN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 2.5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A091552
Product Number: 001
Approval Date: Feb 14, 2011
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information