NDC 70518-3544
Azathioprine 50 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-493.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Baddi Solan, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMar 27, 2024 · 9 inspections |
Product details
- Generic drug
- Azathioprine: every company that makes it
- Form
- tablet, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA208687
- On the market since
- Sep 30, 2022
- Package NDCs
70518-3544-070518-3544-1- Official label
- DailyMed (National Library of Medicine), updated Apr 13, 2026
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