NDC 70166-355
Mupirocin 20 mg per 1 g ointment
On the label: Lohxa. It's repackaged: Lohxa rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-1312.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharma Canada Inc. | Brampton, Canada | Makes it | No problems foundMar 27, 2026 · 7 inspections |
| Taro Pharmaceutical Industries Ltd. | Haifa Bay, Israel | Makes it | No problems foundDec 8, 2022 · 7 inspections |
Repackaging site
- Lohxa LLC, North Oxford, MA, United States · repackages it
Product details
- Generic drug
- Mupirocin: every company that makes it
- Form
- ointment, topical
- Strength
- 20 mg per 1 g
- Approval
- ANDA ANDA065170
- On the market since
- May 26, 2018
- Package NDCs
70166-355-1070166-355-50- Official label
- DailyMed (National Library of Medicine), updated Mar 25, 2025
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