# Lenalidomide

NDC: 43598-513
Generic name: Lenalidomide
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20220907

FDA application: ANDA209348

## Active ingredients

- LENALIDOMIDE: 15 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-513"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-513
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ca8cc2cc-c856-e676-4f60-1e46d7b53d73