Mupirocin
MUPIROCIN OINTMENT USP, 2%
Approved
Approval ID
c624575e-558c-4cfd-b1e0-c262ed11cff9
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 7, 2011
Manufacturers
FDA
Keltman Pharmaceuticals Inc.
DUNS: 362861077
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 Code68387-550
Application NumberANDA065192
Product Classification
M
Marketing Category
C73584
G
Generic Name
mupirocin
Product Specifications
Route of AdministrationTOPICAL
Effective DateJune 7, 2011
FDA Product Classification
INGREDIENTS (3)
MUPIROCINActive
Quantity: 20 mg in 1 g
Code: D0GX863OA5
Classification: ACTIB
POLYETHYLENE GLYCOL 3350Inactive
Code: G2M7P15E5P
Classification: IACT
POLYETHYLENE GLYCOL 400Inactive
Code: B697894SGQ
Classification: IACT