# DULOXETINE HYDROCHLORIDE

NDC: 62332-280
Generic name: Duloxetine
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20260409

FDA application: ANDA202949

## Active ingredients

- DULOXETINE HYDROCHLORIDE: 60 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62332-280"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-280
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=39453971-766d-45bf-a0fd-4658d72bae72