Application 076204

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	MOEXIPRIL HYDROCHLORIDE	MOEXIPRIL HYDROCHLORIDE	TABLET;ORAL	7.5MG	No	No
002	MOEXIPRIL HYDROCHLORIDE	MOEXIPRIL HYDROCHLORIDE	TABLET;ORAL	15MG	No	Yes

NDC, Name, Nonproprietary name table
NDC	Name	Nonproprietary name	Labeler	Marketing category	Status
0093-0017	Moexipril Hydrochloride	Moexipril Hydrochloride	Teva Pharmaceuticals USA, Inc.	ANDA	Current
0093-0017	Moexipril Hydrochloride	Moexipril Hydrochloride	Teva Pharmaceuticals USA, Inc.	ANDA	Current
0093-5150	Moexipril Hydrochloride	Moexipril Hydrochloride	Teva Pharmaceuticals USA, Inc.	ANDA	Current
0093-5150	Moexipril Hydrochloride	Moexipril Hydrochloride	Teva Pharmaceuticals USA, Inc.	ANDA	Current
68151-1472	Moexipril Hydrochloride	Moexipril Hydrochloride	Carilion Materials Management	ANDA	Current
68151-1473	Moexipril Hydrochloride	Moexipril Hydrochloride	Carilion Materials Management	ANDA	Current

Document, Submission type, Date table
Document	Submission type	Date
22548	ORIG	2005-07-22