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: A202600
Product Number: 001
Approval Date: Dec 21, 2012
Applicant Holder Full Name: EUGIA PHARMA SPECIALITIES LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information