NDC 71335-2578
Alfuzosin Hydrochloride 10 mg tablet, film coated, extended release
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-114.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Alfuzosin: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA079060
- On the market since
- Aug 30, 2012
- Package NDCs
71335-2578-171335-2578-271335-2578-371335-2578-471335-2578-5- Official label
- DailyMed (National Library of Medicine), updated May 7, 2026
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