Active Ingredient: IRINOTECAN HYDROCHLORIDE
Proprietary Name: IRINOTECAN HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 100MG/5ML (20MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A091032
Product Number: 002
Approval Date: Dec 20, 2010
Applicant Holder Full Name: HIKMA FARMACEUTICA (PORTUGAL) SA
Marketing Status:
Prescription
Patent and Exclusivity Information