NDC 76420-885
tizanidine 2 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Viona Pharmaceuticals Inc.'s NDC 72578-096.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyMar 24, 2023 · 5 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Tizanidine: every company that makes it
- Form
- tablet, oral
- Strength
- 2 mg
- Approval
- ANDA ANDA208187
- On the market since
- Mar 4, 2021
- Package NDCs
76420-885-0076420-885-0176420-885-1176420-885-1576420-885-2176420-885-3076420-885-6076420-885-8876420-885-9076420-885-99- Official label
- DailyMed (National Library of Medicine), updated Dec 26, 2024
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