United States · FDA National Drug Code directory
Nilotinib
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
- 43598-055_0e4d3a09-2813-d066-3d1b-2a7e0b196fd5
- Product NDC
- 43598-055
- Form
- CAPSULE
- Composition / generic term
- Nilotinib
- Labeler
- Dr. Reddy's Laboratories Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251119
- Source listing expiry
- 20261231
Source-listed ingredients
- NILOTINIB HYDROCHLORIDE MONOHYDRATE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 CAPSULE in 1 BOTTLE (43598-055-04) · 43598-055-04
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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