NDC 71626-999
Probenecid 500 mg tablet, film coated
On the label: Medstone Pharma LLC. It's repackaged: Medstone Pharma LLC rebottles it from Lannett Company, Inc.'s NDC 0527-1367.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lannett Company, LLC | Seymour, IN, United States | Makes it, packages it and labels it | Problems found, fixed voluntarilyOct 21, 2022 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Probenecid: every company that makes it
- Form
- tablet, film coated
- Strength
- 500 mg
- Approval
- ANDA ANDA080966
- On the market since
- Jul 29, 1976
- Package NDCs
71626-999-08- Official label
- DailyMed (National Library of Medicine), updated Sep 4, 2020
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