Class II

Drug Recall: 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,

Glenmark Pharmaceuticals Inc., USA · August 30, 2024

Reason for Recall

Subpotent Drug

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.

Distribution

Product was distributed nationwide within the United States.

States Affected

NATIONWIDE

Quantity Affected

2,031,480 ointments

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0660-2024

Status: completed

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.