MANNITOL 25% Detail

Drug Name(s):
MANNITOL 25%

FDA Application No.:
NDA 080677

Active Ingredient(s):
MANNITOL

Company:
ABRAXIS PHARM

Original Approval or Tentative Approval Date:
November 7, 1982

Products on Application NDA 080677:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
MANNITOL	12.5GM/50ML	INJECTABLE; INJECTION	Prescription	AP

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last updated on 12-05-2008

MANNITOL 25% Detail

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