Application 011552

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	STELAZINE	TRIFLUOPERAZINE HYDROCHLORIDE	TABLET;ORAL	EQ 1MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
002	STELAZINE	TRIFLUOPERAZINE HYDROCHLORIDE	TABLET;ORAL	EQ 2MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
003	STELAZINE	TRIFLUOPERAZINE HYDROCHLORIDE	TABLET;ORAL	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
004	STELAZINE	TRIFLUOPERAZINE HYDROCHLORIDE	TABLET;ORAL	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
005	STELAZINE	TRIFLUOPERAZINE HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 2MG BASE/ML Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
006	STELAZINE	TRIFLUOPERAZINE HYDROCHLORIDE	CONCENTRATE;ORAL	EQ 10MG BASE/ML Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No

Document, Submission type, Date table
Document	Submission type	Date
40672	SUPPL	2003-02-04
269	SUPPL	2001-04-03