NDC 68071-3772
Azathioprine 50 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-003.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Azathioprine: every company that makes it
- Form
- tablet, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA077621
- On the market since
- Jul 11, 2007
- Package NDCs
68071-3772-6- Official label
- DailyMed (National Library of Medicine), updated Jan 13, 2025
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