# Duloxetine Delayed-Release

NDC: 63629-1990
Generic name: DULOXETINE HYDROCHLORIDE
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE PELLETS
Routes: ORAL
Marketing started: 20140611

FDA application: ANDA203088

## Active ingredients

- DULOXETINE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-1990"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-1990
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b25c01e0-273a-4f8f-a37e-9b17e5cf378f