# Pomalidomide

NDC: 0480-4035
Generic name: Pomalidomide
Labeler / Manufacturer: Teva Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20260302

FDA application: ANDA209956

## 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:"0480-4035"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0480-4035
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dee932c5-0c7c-45f0-b2bb-c027badee537