# PALONOSETRON

NDC: 63323-673
Generic name: Palonosetron
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20180919

FDA application: ANDA206802

## Active ingredients

- PALONOSETRON HYDROCHLORIDE: .25 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-673"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-673
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9132366b-b808-46c9-b167-c1900bc116b3