Mupirocin
MUPIROCIN OINTMENT USP, 2%
Approved
Approval ID
a76947bd-0430-4d79-b4c1-9d1746bc7f84
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 6, 2010
Manufacturers
FDA
Rebel Distributors Corp.
DUNS: 118802834
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 Code21695-188
Application NumberANDA065192
Product Classification
M
Marketing Category
C73584
G
Generic Name
mupirocin
Product Specifications
Route of AdministrationTOPICAL
Effective DateNovember 11, 2009
FDA Product Classification
INGREDIENTS (3)
mupirocinActive
Quantity: 20 mg in 1 g
Code: D0GX863OA5
Classification: ACTIB
polyethylene glycol 400Inactive
Code: B697894SGQ
Classification: IACT
polyethylene glycol 3350Inactive
Code: G2M7P15E5P
Classification: IACT