NDC 81033-049
Lidocaine 50 mg per 1 g ointment
On the label: Kesin Pharma Corporation. It's repackaged: Kesin Pharma Corporation rebottles it from Quagen Pharmaceuticals LLC's NDC 70752-113.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Quagen Pharmaceuticals LLC | West Caldwell, NJ, United States | Makes it and packages it | No problems foundApr 17, 2026 · 3 inspections |
Repackaging site
- Kesin Pharma Corporation, Oldsmar, FL, United States · labels it and repackages it
Product details
- Generic drug
- Lidocaine: every company that makes it
- Form
- ointment, topical
- Strength
- 50 mg per 1 g
- Approval
- ANDA ANDA212695
- On the market since
- Apr 20, 2021
- Package NDCs
81033-049-0581033-049-55- Official label
- DailyMed (National Library of Medicine), updated Jul 22, 2026
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