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
16714-834_8d32d892-2cbb-f22e-0084-b405875974af
Product NDC
16714-834
Form
INJECTION, SOLUTION
Composition / generic term
Palonosetron
Labeler
NorthStar Rx LLC
Marketing category
ANDA
Marketing start / end (source format)
20180529
Source listing expiry
20261231

Source-listed ingredients

  • PALONOSETRON HYDROCHLORIDE — .05 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, SINGLE-USE in 1 CARTON (16714-834-01) / 5 mL in 1 VIAL, SINGLE-USE · 16714-834-01

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.

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