# Pomalyst

NDC: 59572-503
Generic name: pomalidomide
Labeler / Manufacturer: Celgene Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20130218

FDA application: NDA204026

## Active ingredients

- POMALIDOMIDE: 3 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59572-503"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59572-503
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2b25ef01-5c9e-11e1-b86c-0800200c9a66
