Active Ingredient: ONDANSETRON HYDROCHLORIDE
Proprietary Name: ONDANSETRON HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 4MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A077306
Product Number: 001
Approval Date: Jun 25, 2007
Applicant Holder Full Name: APOTEX INC
Marketing Status:
Prescription
Patent and Exclusivity Information
