# Duloxetine D/R

NDC: 72189-661
Generic name: Duloxetine D/R
Labeler / Manufacturer: Direct_Rx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20260209

FDA application: ANDA208706

## 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:"72189-661"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-661
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4a66fde2-4cce-b92e-e063-6294a90a63ee