Active Ingredient: ONDANSETRON HYDROCHLORIDE
Proprietary Name: ZOFRAN
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: EQ 4MG BASE/5ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N020605
Product Number: 001
Approval Date: Jan 24, 1997
Applicant Holder Full Name: SANDOZ INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
