NDC 72789-327
Tizanidine 4 mg tablet
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 57664-503.
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 |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Tizanidine: every company that makes it
- Form
- tablet, oral
- Strength
- 4 mg
- Approval
- ANDA ANDA076416
- On the market since
- Dec 11, 2003
- Package NDCs
72789-327-20- Official label
- DailyMed (National Library of Medicine), updated Oct 28, 2026
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