Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 202631
Company: MACLEODS PHARMS LTD

Products on ANDA 202631

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
DONEPEZIL HYDROCHLORIDE	DONEPEZIL HYDROCHLORIDE	23MG	TABLET;ORAL	Prescription	AB	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 202631

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
01/22/2014	ORIG-1	Approval				Label is not available on this site.

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
11/13/2020	SUPPL-11	Labeling-Package Insert, Labeling-Patient Package Insert		Label is not available on this site.
11/08/2016	SUPPL-6	Labeling-Package Insert		Label is not available on this site.
09/22/2016	SUPPL-3	Labeling-Package Insert		Label is not available on this site.

Therapeutic Equivalents for ANDA 202631

DONEPEZIL HYDROCHLORIDE

TABLET;ORAL; 23MG
TE Code = AB

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
ARICEPT	DONEPEZIL HYDROCHLORIDE	23MG	TABLET;ORAL	Prescription	Yes	AB	022568	EISAI INC
DONEPEZIL HYDROCHLORIDE	DONEPEZIL HYDROCHLORIDE	23MG	TABLET;ORAL	Prescription	No	AB	203713	DEXCEL
DONEPEZIL HYDROCHLORIDE	DONEPEZIL HYDROCHLORIDE	23MG	TABLET;ORAL	Prescription	No	AB	202723	DR REDDYS
DONEPEZIL HYDROCHLORIDE	DONEPEZIL HYDROCHLORIDE	23MG	TABLET;ORAL	Prescription	No	AB	202631	MACLEODS PHARMS LTD
DONEPEZIL HYDROCHLORIDE	DONEPEZIL HYDROCHLORIDE	23MG	TABLET;ORAL	Prescription	No	AB	203104	TWI PHARMS
DONEPEZIL HYDROCHLORIDE	DONEPEZIL HYDROCHLORIDE	23MG	TABLET;ORAL	Prescription	No	AB	203162	ZYDUS PHARMS