Cefoxitin

Product NDC

60505-0759

11-digit product format

605050759

Labeler code

60505

Product ID

60505-0759_c59ccfb3-75a5-43d3-b3e4-c99f20f3d074

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

CEFOXITIN

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Apotex Corporation

Application

ANDA065313

Marketing category

ANDA

Marketing start

2006-02-13

Marketing end

0000-00-00

Substance

CEFOXITIN SODIUM

Active strength

1 g/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record