# Duloxetine HCL DR

NDC: 80425-0012
Generic name: Duloxetine HCL
Labeler / Manufacturer: Advanced Rx of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20120501

FDA application: ANDA203197

## 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:"80425-0012"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0012
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=af6f8abd-19ec-69e4-e053-2a95a90ab69e