Active Ingredient: DONEPEZIL HYDROCHLORIDE
Proprietary Name: DONEPEZIL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A204609
Product Number: 002
Approval Date: Sep 19, 2017
Applicant Holder Full Name: CADILA PHARMACEUTICALS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
