LACTULOSE Detail

Drug Name(s):
LACTULOSE

FDA Application No.:
NDA 073591

Active Ingredient(s):
LACTULOSE

Company:
ROXANE

Original Approval or Tentative Approval Date:
August 17, 1995

Products on Application NDA 073591:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
LACTULOSE	10GM/15ML	SOLUTION; ORAL	Prescription	AA

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last updated on 12-01-2008

LACTULOSE Detail

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