Active Ingredient: DONEPEZIL HYDROCHLORIDE
Proprietary Name: DONEPEZIL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, ORALLY DISINTEGRATING; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077975
Product Number: 001
Approval Date: Dec 11, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
