NDC 67296-2316
Tizanidine 2 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Northstar Rx LLC.'s NDC 16714-171.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Srikakulam, India | Makes it and tests it | Problems found, fixed voluntarilyMay 20, 2022 · 5 inspections |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Tizanidine: every company that makes it
- Form
- tablet, oral
- Strength
- 2 mg
- Approval
- ANDA ANDA076286
- On the market since
- Jun 15, 2021
- Package NDCs
67296-2316-4- Official label
- DailyMed (National Library of Medicine), updated Aug 25, 2026
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