NDC 81033-020
Mupirocin 20 mg per 1 g ointment
On the label: Kesin Pharma Corporation. It's repackaged: Kesin Pharma Corporation rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-180.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Goa, India | Makes it and tests it | Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action |
Repackaging site
- Kesin Pharma Corporation, Oldsmar, FL, United States · repackages it
Recalls
- Aug 30, 2024 · Class II · Glenmark Pharmaceuticals Inc., USA
Subpotent Drug
Lots: Lot #: 19223615, 19223537, 19223544,19223568, 19223593,19223641, Exp. Date 08/2024; 19224055,19224281, 19224307, 19224321, 19224341, 19224467, Exp. Date 09/2024; 19224525, 19224542, 19224560,19224580, Exp. Date 10/2024; 19224990, 19224998, 19225014, 19225033, 19225293, 19225304, 19225320, 192253…
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Mupirocin: every company that makes it
- Form
- ointment
- Strength
- 20 mg per 1 g
- Approval
- ANDA ANDA090480
- On the market since
- Oct 15, 2021
- Package NDCs
81033-020-0181033-020-5081033-020-99- Official label
- DailyMed (National Library of Medicine), updated May 28, 2025
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