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
67184-0515_abeff9bd-6829-445c-93b8-3d9217993b9c
Product NDC
67184-0515
Form
INJECTION
Composition / generic term
Palonosetron Hydrochloride
Labeler
Qilu Pharmaceutical Co., Ltd.
Marketing category
ANDA
Marketing start / end (source format)
20180919
Source listing expiry
20261231

Source-listed ingredients

  • PALONOSETRON HYDROCHLORIDE — .075 mg/1.5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 5 VIAL in 1 CARTON (67184-0515-2) / 1.5 mL in 1 VIAL (67184-0515-1) · 67184-0515-2

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →