Dermawerx Surgical PrePak
Dermawerx Surgical PrePak
Approved
Approval ID
2687330c-50dc-0339-e054-00144ff88e88
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 10, 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.
chlorhexidine gluconate pre-surgical kit
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code69329-260
Application NumberNDA019125
Product Classification
M
Marketing Category
C73594
G
Generic Name
chlorhexidine gluconate pre-surgical kit
Product Specifications
Route of AdministrationTOPICAL
Effective DateDecember 10, 2015
FDA Product Classification