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: Yes
TE Code: AB
Application Number: A201787
Product Number: 002
Approval Date: Dec 14, 2012
Applicant Holder Full Name: MACLEODS PHARMACEUTICALS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information