MUPIROCIN
Approved
Approval ID
dc6c7600-454b-449f-af1c-ff1a8e1b8109
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 9, 2010
Manufacturers
FDA
STAT RX LLC USA
DUNS: 786036330
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 Code16590-158
Application NumberANDA065123
Product Classification
M
Marketing Category
C73584
G
Generic Name
MUPIROCIN
Product Specifications
Route of AdministrationTOPICAL
Effective DateJune 9, 2010
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 3500Inactive
Code: FVS1AZD90Y
Classification: IACT