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Last Updated: December 18, 2025

Details for New Drug Application (NDA): 077536

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NDA 077536 describes MOEXIPRIL HYDROCHLORIDE, which is a drug marketed by Apotex Inc, Chartwell Rx, Glenmark Pharms Ltd, Teva, Glenmark Pharms, and Heritage, and is included in eight NDAs. It is available from three suppliers. Additional details are available on the MOEXIPRIL HYDROCHLORIDE profile page.

The generic ingredient in MOEXIPRIL HYDROCHLORIDE is hydrochlorothiazide; moexipril hydrochloride. There are thirty-two drug master file entries for this compound. Additional details are available on the hydrochlorothiazide; moexipril hydrochloride profile page.

Summary for 077536

Tradename:	MOEXIPRIL HYDROCHLORIDE
Applicant:	Chartwell Rx
Ingredient:	moexipril hydrochloride
Patents:	0

Pharmacology for NDA: 077536

Mechanism of Action	Angiotensin-converting Enzyme Inhibitors

Suppliers and Packaging for NDA: 077536

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
MOEXIPRIL HYDROCHLORIDE	moexipril hydrochloride	TABLET;ORAL	077536	ANDA	Chartwell RX, LLC	62135-967	62135-967-90	90 TABLET, FILM COATED in 1 BOTTLE (62135-967-90)
MOEXIPRIL HYDROCHLORIDE	moexipril hydrochloride	TABLET;ORAL	077536	ANDA	Chartwell RX, LLC	62135-969	62135-969-90	90 TABLET, FILM COATED in 1 BOTTLE (62135-969-90)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	7.5MG
Approval Date:	Nov 30, 2006	TE:	AB	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	15MG
Approval Date:	Nov 30, 2006	TE:	AB	RLD:	No

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