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Last Updated: December 14, 2024

Details for New Drug Application (NDA): 090551


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NDA 090551 describes DONEPEZIL HYDROCHLORIDE, which is a drug marketed by Chartwell Rx, Hisun Pharm Hangzhou, Macleods Pharms Ltd, Sandoz, Sun Pharm Industries, Unichem, Zydus Pharms Usa Inc, Accord Hlthcare, Actavis Elizabeth, Alembic Pharms Ltd, Apotex, Aurobindo, Cadila Pharms Ltd, Cipla Ltd, Dexcel, Dr Reddys, Dr Reddys Labs Ltd, Endo Operations, Esjay Pharma, Heritage Pharma, Hetero Labs Ltd V, Hikma Pharms, Indicus Pharma, Jubilant Generics, Lupin Ltd, Natco Pharma, Osmotica Pharm Us, Prinston Inc, Rising, Sciegen Pharms Inc, Strides Pharma, Sun Pharm, Sun Pharm Inds, Sun Pharm Inds Ltd, Torrent Pharms, Twi Pharms, Wockhardt, Zydus Lifesciences, and Zydus Pharms, and is included in forty-seven NDAs. It is available from thirty-seven suppliers. Additional details are available on the DONEPEZIL HYDROCHLORIDE profile page.

The generic ingredient in DONEPEZIL HYDROCHLORIDE is donepezil hydrochloride. There are thirty-two drug master file entries for this compound. Thirty-nine suppliers are listed for this compound. Additional details are available on the donepezil hydrochloride profile page.
Summary for 090551
Tradename:DONEPEZIL HYDROCHLORIDE
Applicant:Esjay Pharma
Ingredient:donepezil hydrochloride
Patents:0
Pharmacology for NDA: 090551
Mechanism of ActionCholinesterase Inhibitors
Suppliers and Packaging for NDA: 090551
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
DONEPEZIL HYDROCHLORIDE donepezil hydrochloride TABLET;ORAL 090551 ANDA Strides Pharma Science Limited 64380-907 64380-907-04 30 TABLET, FILM COATED in 1 BOTTLE (64380-907-04)
DONEPEZIL HYDROCHLORIDE donepezil hydrochloride TABLET;ORAL 090551 ANDA Strides Pharma Science Limited 64380-907 64380-907-05 90 TABLET, FILM COATED in 1 BOTTLE (64380-907-05)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength5MG
Approval Date:May 31, 2011TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength10MG
Approval Date:May 31, 2011TE:ABRLD:No

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