# Duloxetine

NDC: 70954-861
Generic name: Duloxetine
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20260713

FDA application: ANDA202336

## Active ingredients

- DULOXETINE HYDROCHLORIDE: 30 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70954-861"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70954-861
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fb37745f-fb40-4f7f-8143-ea1874c38e1b