MANNITOL 5% Detail

Drug Name(s):
MANNITOL 5%

FDA Application No.:
NDA 016080

Active Ingredient(s):
MANNITOL

Company:
B BRAUN

Original Approval or Tentative Approval Date:
August 7, 1977

Products on Application NDA 016080:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
MANNITOL	15GM/100ML	INJECTABLE; INJECTION	Prescription	AP
MANNITOL	15GM/100ML	INJECTABLE; INJECTION	Prescription	AP
MANNITOL	5GM/100ML	INJECTABLE; INJECTION	Prescription	AP
MANNITOL	5GM/100ML	INJECTABLE; INJECTION	Prescription	AP

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last updated on 11-21-2008

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