United States · FDA National Drug Code directory

DANZITEN

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
24338-155_62029a35-74af-47bc-9b7b-93dcaddfd278
Product NDC
24338-155
Form
TABLET
Composition / generic term
nilotinib
Labeler
Azurity Pharmaceuticals, Inc.
Marketing category
NDA
Marketing start / end (source format)
20241130
Source listing expiry
20261231

Source-listed ingredients

  • NILOTINIB — 95 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 4 CARTON in 1 CARTON (24338-155-01) / 2 BLISTER PACK in 1 CARTON (24338-155-02) / 14 TABLET in 1 BLISTER PACK (24338-155-03) · 24338-155-01

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.

Browse United States records →