NDC 70518-3658
Tizanidine 4 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Northstar Rx LLC.'s NDC 16714-172.
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 |
Product details
- Generic drug
- Tizanidine: every company that makes it
- Form
- tablet, oral
- Strength
- 4 mg
- Approval
- ANDA ANDA076286
- On the market since
- Feb 23, 2023
- Package NDCs
70518-3658-070518-3658-170518-3658-270518-3658-3- Official label
- DailyMed (National Library of Medicine), updated Aug 14, 2026
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