# Pomalidomide

NDC: 0781-2369
Generic name: pomalidomide
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20260901

FDA application: ANDA220741

## Active ingredients

- POMALIDOMIDE: 4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-2369"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-2369
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4fcd4978-b2d1-4d1a-b239-717cddb8be1f