Active Ingredient: LACTULOSE
Proprietary Name: CHRONULAC
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: 10GM/15ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N017884
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SANOFI AVENTIS US LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
