United States · FDA National Drug Code directory

Nintedanib

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
69097-639_128511d3-f076-4a68-993b-53ad52233ee2
Product NDC
69097-639
Form
CAPSULE
Composition / generic term
Nintedanib
Labeler
Cipla USA Inc.
Marketing category
ANDA
Marketing start / end (source format)
20260402
Source listing expiry
20271231

Source-listed ingredients

  • NINTEDANIB ESYLATE — 150 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 CAPSULE in 1 BOTTLE (69097-639-03) · 69097-639-03

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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