# Tasimelteon

NDC: 0480-4490
Generic name: Tasimelteon
Labeler / Manufacturer: Teva Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, GELATIN COATED
Routes: ORAL
Marketing started: 20221229

FDA application: ANDA211601

## Active ingredients

- TASIMELTEON: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0480-4490"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0480-4490
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ce5a2fa3-ed54-422d-96c2-1821496eb32f