# Duloxetine HCL DR

NDC: 80425-0014
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: 20221211

FDA application: ANDA090778

## 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:"80425-0014"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0014
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=afd59273-75cb-5f33-e053-2995a90ab25f