NDC 51655-087
Alfuzosin Hydrochloride 10 mg tablet, film coated, extended release
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals 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
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages 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
- Oct 4, 2022
- Package NDCs
51655-087-52- Official label
- DailyMed (National Library of Medicine), updated Dec 26, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?