Glenmark Pharmaceuticals Limited
Goa, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Jun 30, 2026. 7 inspections on record, 1 with serious problems.
NDC 50436-0180
Mupirocin 20 mg per 1 g ointment
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-180.
Where the pills inside were made
Repackaging site
- Unit Dose Services, · repackages it and relabels it
Recalls
- Aug 30, 2024 · Class II · Completed
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…
Product details
- Generic drug
- Mupirocin: see every company that makes it
- Form
- ointment
- Strength
- 20 mg per 1 g
- Approval
- ANDA ANDA090480
- On the market since
- Jun 8, 2011
- Package NDCs
50436-0180-1- Official label
- DailyMed (National Library of Medicine), updated Jan 2, 2019
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