NDC 57237-114
Alfuzosin Hydrochloride 10 mg tablet, film coated, extended release
On the label: Rising Pharma Holdings, Inc..
Where it's 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 |
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
57237-114-0157237-114-0557237-114-90- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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