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Last Updated: December 22, 2024

Details for New Drug Application (NDA): 202723

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NDA 202723 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 202723

Tradename:	DONEPEZIL HYDROCHLORIDE
Applicant:	Dr Reddys
Ingredient:	donepezil hydrochloride
Patents:	0

Pharmacology for NDA: 202723

Mechanism of Action	Cholinesterase Inhibitors

Suppliers and Packaging for NDA: 202723

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
DONEPEZIL HYDROCHLORIDE	donepezil hydrochloride	TABLET;ORAL	202723	ANDA	Dr. Reddys Laboratories Limited	55111-302	55111-302-05	500 TABLET, FILM COATED in 1 BOTTLE (55111-302-05)
DONEPEZIL HYDROCHLORIDE	donepezil hydrochloride	TABLET;ORAL	202723	ANDA	Dr. Reddys Laboratories Limited	55111-302	55111-302-10	1000 TABLET, FILM COATED in 1 BOTTLE (55111-302-10)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	23MG
Approval Date:	Jul 24, 2013	TE:	AB	RLD:	No

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