United States · FDA National Drug Code directory

Lenalidomide

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
73043-043_0835d82d-196b-4ec8-aa3b-adb7fe501aa2
Product NDC
73043-043
Form
CAPSULE
Composition / generic term
Lenalidomide
Labeler
Devatis Inc.
Marketing category
ANDA
Marketing start / end (source format)
20260131
Source listing expiry
20271231

Source-listed ingredients

  • LENALIDOMIDE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE in 1 BOTTLE (73043-043-01) · 73043-043-01
  • 21 CAPSULE in 1 BOTTLE (73043-043-21) · 73043-043-21

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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