Active Ingredient: PALONOSETRON HYDROCHLORIDE
Proprietary Name: PALONOSETRON HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION; INTRAVENOUS
Strength: EQ 0.25MG BASE/5ML (EQ 0.05MG BASE/ML)
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N208109
Product Number: 001
Approval Date: Nov 21, 2017
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information