MANNITOL 10% Detail

Drug Name(s):
MANNITOL 10%

FDA Application No.:
NDA 016269

Active Ingredient(s):
MANNITOL

Company:
HOSPIRA

Original Approval or Tentative Approval Date:
February 29, 1976

Products on Application NDA 016269:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
MANNITOL	10GM/100ML	INJECTABLE; INJECTION	Discontinued	none
MANNITOL	12.5GM/50ML	INJECTABLE; INJECTION	Prescription	AP
MANNITOL	20GM/100ML	INJECTABLE; INJECTION	Discontinued	none

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last updated on 11-21-2008

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