# Tamsulosin Hydrochloride

NDC: 71335-0398
Generic name: Tamsulosin Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20130430

FDA application: ANDA202433

## Active ingredients

- TAMSULOSIN HYDROCHLORIDE: .4 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-0398"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-0398
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=58bdac81-680a-4fd2-8f05-dd5b86553569