Mupirocin Ointment, USP, 2%, 22 g, Rx only, Manufactured by: Glenmark Pharmaceuticals, Ltd., Colvale-Bardez, Goa 403513, India. Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ, 07430, NDC 68462-180-22.
Reported: October 2, 2024 Initiated: August 30, 2024 #D-0660-2024
Product Description
Mupirocin Ointment, USP, 2%, 22 g, Rx only, Manufactured by: Glenmark Pharmaceuticals, Ltd., Colvale-Bardez, Goa 403513, India. Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ, 07430, NDC 68462-180-22.
Reason for Recall
Subpotent Drug
Details
- Recalling Firm
- Glenmark Pharmaceuticals Inc., USA
- Units Affected
- 2,031,480 ointments
- Distribution
- Product was distributed nationwide within the United States.
- Location
- Mahwah, NJ
Frequently Asked Questions
What product was recalled? ▼
Mupirocin Ointment, USP, 2%, 22 g, Rx only, Manufactured by: Glenmark Pharmaceuticals, Ltd., Colvale-Bardez, Goa 403513, India. Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ, 07430, NDC 68462-180-22.. Recalled by Glenmark Pharmaceuticals Inc., USA. Units affected: 2,031,480 ointments.
Why was this product recalled? ▼
Subpotent Drug
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 2, 2024. Severity: Moderate. Recall number: D-0660-2024.
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