Active Ingredient: LACTULOSE
Proprietary Name: LACTULOSE
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: 10GM/15ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A073591
Product Number: 001
Approval Date: May 29, 1992
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information