United States · FDA National Drug Code directory

Bosutinib

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
46708-312_17a3b455-b49a-492d-b6dc-47e96e6037ed
Product NDC
46708-312
Form
TABLET, FILM COATED
Composition / generic term
Bosutinib
Labeler
Alembic Pharmaceuticals Limited
Marketing category
ANDA
Marketing start / end (source format)
20260519
Source listing expiry
20271231

Source-listed ingredients

  • BOSUTINIB — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED in 1 BOTTLE (46708-312-30) · 46708-312-30

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 →