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:
Application Number: A076780
Product Number: 001
Approval Date: Dec 26, 2006
Applicant Holder Full Name: HIKMA FARMACEUTICA (PORTUGAL) SA
Marketing Status:
Discontinued
Patent and Exclusivity Information