United States · FDA National Drug Code directory
Palonosetron
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 68001-708_55f40e1d-3da6-3579-e063-6394a90a1ea5
- Product NDC
- 68001-708
- Form
- INJECTION
- Composition / generic term
- Palonosetron Hydrochloride
- Labeler
- BLuePoint Laboratories
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260715
- Source listing expiry
- 20271231
Source-listed ingredients
- PALONOSETRON HYDROCHLORIDE — .25 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 CARTON (68001-708-25) / 5 mL in 1 VIAL · 68001-708-25
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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