# duloxetine

NDC: 49252-009
Generic name: duloxetine
Labeler / Manufacturer: Inventia Healthcare Limited.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20151205

FDA application: ANDA202336

## 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:"49252-009"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49252-009
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=eab90059-ea1c-46c1-884d-c15e7c562a01