# Duloxetine

NDC: 55700-727
Generic name: Duloxetine
Labeler / Manufacturer: Quality Care Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20190222
Marketing ended: 20260531
FDA application: ANDA208706

## Active ingredients

- DULOXETINE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55700-727"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55700-727
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4d489d05-e767-498f-8827-c03ebfc512e0