mupirocin
These highlights do not include all the information needed to use safely and effectively. See full prescribing information for . MUPIROCIN ointment, for topical useInitial U.S. Approval: 1987
Approved
Approval ID
0b57affe-8fa3-4517-adfd-1b0d938e72eb
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 25, 2021
Manufacturers
FDA
A-S Medication Solutions
DUNS: 830016429
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Mupirocin
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code50090-4349
Application NumberANDA065123
Product Classification
M
Marketing Category
C73584
G
Generic Name
Mupirocin
Product Specifications
Route of AdministrationTOPICAL
Effective DateDecember 9, 2019
FDA Product Classification
INGREDIENTS (2)
POLYETHYLENE GLYCOL, UNSPECIFIEDInactive
Code: 3WJQ0SDW1A
Classification: IACT
MUPIROCINActive
Quantity: 20 mg in 1 g
Code: D0GX863OA5
Classification: ACTIB