Active Ingredient: FLOXURIDINE
Proprietary Name: FLOXURIDINE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 500MG/VIAL
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AP
Application Number: A075387
Product Number: 001
Approval Date: Apr 16, 2000
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information