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: AA
Application Number: A091342
Product Number: 001
Approval Date: Jan 27, 2011
Applicant Holder Full Name: CHARTWELL MOLECULAR HOLDINGS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information