MANNITOL 5% IN PLASTIC CONTAINER Detail

Drug Name(s):
MANNITOL 5% IN PLASTIC CONTAINER

FDA Application No.:
NDA 020006

Active Ingredient(s):
MANNITOL

Company:
B BRAUN

Original Approval or Tentative Approval Date:
July 25, 1993

Products on Application NDA 020006:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
MANNITOL	15GM/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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