NDC 81033-068
Moxifloxacin 400 mg tablet, film coated
On the label: Kesin Pharma Corporation. It's repackaged: Kesin Pharma Corporation rebottles it from Solaris Pharma Corporation's NDC 73473-903.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sunshine Lake Pharma Co., Ltd. | Dongguan, China | Makes it | Problems found, fixed voluntarilyMar 22, 2024 · 5 inspections, 1 with FDA action |
Repackaging site
- Kesin Pharma Corporation, Oldsmar, FL, United States · packages it, labels it and repackages it
Product details
- Generic drug
- Moxifloxacin: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 400 mg
- Approval
- ANDA ANDA206295
- On the market since
- Dec 12, 2025
- Package NDCs
81033-068-3181033-068-51- Official label
- DailyMed (National Library of Medicine), updated Nov 6, 2026
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