NDC 67046-022
Allopurinol 100 mg tablet
On the label: Coupler Enterprises Inc.. It's repackaged: Coupler Enterprises Inc. 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
- Coupler Enterprises, Location not on file · repackages it
Product details
- Generic drug
- Allopurinol: every company that makes it
- Form
- tablet
- Strength
- 100 mg
- Approval
- ANDA ANDA071450
- On the market since
- Jan 9, 1987
- Package NDCs
67046-022-30- Official label
- DailyMed (National Library of Medicine), updated Aug 30, 2017
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