NDC 70518-3181
Tizanidine 2 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 57664-502.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ALKALOIDA Vegyeszeti Gyar zartkoruen mukodo Reszvenytarsasag | Tiszavasvari, Hungary | Makes it, tests it and packages it | Problems found, fixed voluntarilyMar 12, 2025 · 6 inspections |
Product details
- Generic drug
- Tizanidine: every company that makes it
- Form
- tablet, oral
- Strength
- 2 mg
- Approval
- ANDA ANDA076416
- On the market since
- Aug 5, 2021
- Package NDCs
70518-3181-070518-3181-1- Official label
- DailyMed (National Library of Medicine), updated Apr 6, 2026
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