# Duloxetine

NDC: 70518-1054
Generic name: Duloxetine
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20180309

FDA application: ANDA208706

## Active ingredients

- DULOXETINE HYDROCHLORIDE: 30 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-1054"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-1054
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b149641a-03e6-4fee-91f3-7ba8e01196bd