Application 015921

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	HALDOL	HALOPERIDOL	TABLET;ORAL	0.5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
002	HALDOL	HALOPERIDOL	TABLET;ORAL	1MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
003	HALDOL	HALOPERIDOL	TABLET;ORAL	2MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
004	HALDOL	HALOPERIDOL	TABLET;ORAL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
005	HALDOL	HALOPERIDOL	TABLET;ORAL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
006	HALDOL	HALOPERIDOL	TABLET;ORAL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No