# Duloxetine

NDC: 59651-282
Generic name: Duloxetine Hydrochloride
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20131211

FDA application: ANDA090778

## 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:"59651-282"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-282
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3adfceb3-5f89-4bcf-b874-e3cb572a98b6