Cefoxitin

Product NDC

63323-343

11-digit product format

633230343

Labeler code

63323

Product ID

63323-343_924ce0b3-fa14-62a3-e053-2995a90a15a4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefoxitin

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Fresenius Kabi USA, LLC

Application

ANDA065415

Marketing category

ANDA

Marketing start

2012-02-21

Marketing end

2019-10-31

Substance

CEFOXITIN SODIUM

Active strength

10 g/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record