Active Ingredient: ONDANSETRON HYDROCHLORIDE
Proprietary Name: ONDANSETRON HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: EQ 4MG BASE/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078127
Product Number: 001
Approval Date: Jun 25, 2007
Applicant Holder Full Name: PHARMACEUTICAL ASSOCIATES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information