Mupirocin
MUPIROCIN OINTMENT USP, 2%
Approved
Approval ID
e2ddaea4-d914-4bc7-8913-351e7bf2e2f7
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 2, 2009
Manufacturers
FDA
Physicians Total Care, Inc.
DUNS: 194123980
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 Code54868-4958
Application NumberANDA065192
Product Classification
M
Marketing Category
C73584
G
Generic Name
mupirocin
Product Specifications
Route of AdministrationTOPICAL
Effective DateJuly 2, 2010
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