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Active Ingredient: IRINOTECAN HYDROCHLORIDE
Proprietary Name: IRINOTECAN HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 40MG/2ML (20MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A077776
Product Number: 001
Approval Date: Feb 27, 2008
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
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: A077776
Product Number: 002
Approval Date: Feb 27, 2008
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information