Mupirocin
These highlights do not include all the information needed to use MUPIROCIN OINTMENT safely and effectively. See full prescribing information for MUPIROCIN OINTMENT. MUPIROCIN ointment, for topical use Initial U.S. Approval: 1987
Approved
Approval ID
6d59e35c-b262-7940-e053-2991aa0a8908
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 10, 2019
Manufacturers
FDA
Lohxa
DUNS: 079872715
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Mupirocin
PRODUCT DETAILS
NDC Product Code70166-355
Application NumberANDA065170
Marketing CategoryC73584
Route of AdministrationTOPICAL
Effective DateSeptember 10, 2019
Generic NameMupirocin
INGREDIENTS (3)
POLYETHYLENE GLYCOL 400Inactive
Code: B697894SGQ
Classification: IACT
POLYETHYLENE GLYCOL 3350Inactive
Code: G2M7P15E5P
Classification: IACT
MUPIROCINActive
Quantity: 20 mg in 1 g
Code: D0GX863OA5
Classification: ACTIB