FRESENIUS KABI USA Application 080677

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	MANNITOL 25%	MANNITOL	INJECTABLE;INJECTION	12.5GM/50ML	No	No

NDC, Name, Nonproprietary name table
NDC	Name	Nonproprietary name	Labeler	Marketing category	Status
63323-024	Mannitol	MANNITOL	Fresenius Kabi USA, LLC	ANDA	Current
63323-024	Mannitol	MANNITOL	Fresenius Kabi USA, LLC	ANDA	Current