# Duloxetine

NDC: 0228-2891
Generic name: Duloxetine
Labeler / Manufacturer: Actavis Pharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE PELLETS
Routes: ORAL
Marketing started: 20131217

FDA application: ANDA090776

## Active ingredients

- DULOXETINE HYDROCHLORIDE: 30 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0228-2891"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0228-2891
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9dab9154-b86f-40dc-a4d1-18e6534dbc78