Active Ingredient: PROPOFOL
Proprietary Name: PROPOFOL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 10MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A074848
Product Number: 001
Approval Date: Apr 19, 2005
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information