NDC 76420-865
Tizanidine 2 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, 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
- 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 ANDA076286
- On the market since
- Jun 15, 2021
- Package NDCs
76420-865-1276420-865-1576420-865-3076420-865-6076420-865-90- Official label
- DailyMed (National Library of Medicine), updated Oct 29, 2024
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