NDC 51655-082
Allopurinol 100 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 53489-156.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ALKALOIDA Vegyeszeti Gyar zartkoruen mukodo Reszvenytarsasag | Tiszavasvari, Hungary | Makes it | Problems found, fixed voluntarilyMar 12, 2025 · 6 inspections |
| Frontida BioPharm, LLC | Philadelphia, PA, United States | Makes it, tests it and packages it | No problems foundApr 2, 2026 · 10 inspections, 1 with FDA action |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Allopurinol: every company that makes it
- Form
- tablet, oral
- Strength
- 100 mg
- Approval
- ANDA ANDA071450
- On the market since
- Mar 6, 2023
- Package NDCs
51655-082-52- Official label
- DailyMed (National Library of Medicine), updated Dec 26, 2025
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