NDC 68071-2236
Alprazolam 0.25 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Breckenridge Pharmaceutical, Inc.'s NDC 51991-704.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Centaur Pharmaceuticals Private Limited | Pune, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 8, 2023 · 5 inspections, 1 with FDA action |
| Centaur Pharmaceuticals Private Limited | Pernem, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyNov 14, 2025 · 1 inspection |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Alprazolam: every company that makes it
- Form
- tablet
- Strength
- 0.25 mg
- Approval
- ANDA ANDA207507
- On the market since
- Jul 9, 2018
- Package NDCs
68071-2236-6- Official label
- DailyMed (National Library of Medicine), updated Jul 17, 2024
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