MANNITOL 20% Detail

Drug Name(s):
MANNITOL 20%

FDA Application No.:
NDA 014738

Active Ingredient(s):
MANNITOL

Company:
B BRAUN

Original Approval or Tentative Approval Date:
August 9, 1977

Products on Application NDA 014738:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
MANNITOL	20GM/100ML	INJECTABLE; INJECTION	Prescription	AP

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last updated on 11-21-2008

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