# Dutasteride and Tamsulosin Hydrochloride

NDC: 10370-280
Generic name: Dutasteride and Tamsulosin Hydrochloride
Labeler / Manufacturer: Endo USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20151118

FDA application: ANDA202509

## Active ingredients

- DUTASTERIDE: .5 mg/1
- TAMSULOSIN HYDROCHLORIDE: .4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"10370-280"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10370-280
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8c6031b3-b6a8-4ec7-b0d3-286f50d29353