LACTULOSE Detail

Drug Name(s):
LACTULOSE

FDA Application No.:
NDA 074076

Active Ingredient(s):
LACTULOSE

Company:
HI TECH PHARMA

Original Approval or Tentative Approval Date:
October 7, 1997

Products on Application NDA 074076:

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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