# Palonosetron

NDC: 68001-708
Generic name: Palonosetron Hydrochloride
Labeler / Manufacturer: BLuePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20260715

FDA application: ANDA205648

## Active ingredients

- PALONOSETRON HYDROCHLORIDE: .25 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-708"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-708
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bb2be46a-56f7-48b6-bb05-3c6b12c8b1ea