LACTULOSE Detail

Drug Name(s):
LACTULOSE

FDA Application No.:
NDA 074712

Active Ingredient(s):
LACTULOSE

Company:
INALCO

Original Approval or Tentative Approval Date:
December 9, 1997

Products on Application NDA 074712:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
LACTULOSE	20GM/PACKET	FOR SOLUTION; ORAL	Prescription	none

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last updated on 12-01-2008

LACTULOSE Detail

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