Active Ingredient: LACTULOSE
Proprietary Name: LACTULOSE
Dosage Form; Route of Administration: SOLUTION; ORAL, RECTAL
Strength: 10GM/15ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A072029
Product Number: 001
Approval Date: Aug 25, 1992
Applicant Holder Full Name: PACO PHARMACEUTICAL SERVICES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information