MANNITOL 25% Detail

Drug Name(s):
MANNITOL 25%

FDA Application No.:
NDA 086754

Active Ingredient(s):
MANNITOL

Company:
ABRAXIS PHARM

Products on Application NDA 086754:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
MANNITOL	12.5GM/50ML	INJECTABLE; INJECTION	Discontinued	none

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last updated on 12-05-2008

MANNITOL 25% Detail

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