# Duloxetine

NDC: 52427-913
Generic name: Duloxetine
Labeler / Manufacturer: Almatica Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20260701

FDA application: NDA219131

## Active ingredients

- DULOXETINE HYDROCHLORIDE: 90 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"52427-913"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52427-913
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bb2ca3bf-983c-1e4a-a91d-dc7dee66d741