Dermawerx Surgical Plus Pak
Dermawerx Surgical Plus Pak
Approved
Approval ID
268023e4-43f0-3d4c-e054-00144ff8d46c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 9, 2015
Manufacturers
FDA
Patchwerx Labs, Inc.
DUNS: 079584480
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Mupirocin Ointment Kit
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code69329-270
Application NumberANDA065123
Product Classification
M
Marketing Category
C73584
G
Generic Name
Mupirocin Ointment Kit
Product Specifications
Route of AdministrationTOPICAL
Effective DateDecember 9, 2015
FDA Product Classification