# Duloxetine Delayed-Release

NDC: 50090-6889
Generic name: DULOXETINE HYDROCHLORIDE
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE PELLETS
Routes: ORAL
Marketing started: 20140611

FDA application: ANDA203088

## Active ingredients

- DULOXETINE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-6889"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-6889
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=be33f3cb-6fd1-4377-816e-84bd49370e9e