# Dutasteride and tamsulosin hydrochloride

NDC: 70771-1356
Generic name: Dutasteride and tamsulosin hydrochloride
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20180604

FDA application: ANDA207769

## 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:"70771-1356"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1356
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4b89b07e-9d19-47a2-bd53-bc5eef9deed1