Cefoxitin
Cefoxitin for Injection, USP
Approved
Approval ID
f5288962-caee-4771-8229-df9cdefcfa67
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 16, 2023
Manufacturers
FDA
WG Critical Care, LLC
DUNS: 829274633
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Cefoxitin
PRODUCT DETAILS
NDC Product Code44567-247
Application NumberANDA065415
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS
Effective DateOctober 16, 2023
Generic NameCefoxitin
INGREDIENTS (2)
CEFOXITIN SODIUMActive
Quantity: 10 g in 1 1
Code: Q68050H03T
Classification: ACTIM
NATURAL LATEX RUBBERInactive
Quantity: 0 1 in 1 1
Code: 2LQ0UUW8IN
Classification: CNTM