Active Ingredient: ONDANSETRON HYDROCHLORIDE
Proprietary Name: ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A076972
Product Number: 001
Approval Date: Dec 26, 2006
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information