NDC 76420-886
tizanidine 4 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Viona Pharmaceuticals Inc.'s NDC 72578-097.
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
- 4 mg
- Approval
- ANDA ANDA208187
- On the market since
- Mar 4, 2021
- Package NDCs
76420-886-0076420-886-0176420-886-0376420-886-1176420-886-1576420-886-2176420-886-3076420-886-6076420-886-8876420-886-9076420-886-99- Official label
- DailyMed (National Library of Medicine), updated Dec 26, 2024
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