Cefuroxime

Product NDC

44567-711

11-digit product format

445670711

Labeler code

44567

Product ID

44567-711_4d14b1a4-39d2-4e96-b84d-e193fbc99b16

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefuroxime

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAVENOUS

Labeler

WG Critical Care, LLC

Application

ANDA064125

Marketing category

ANDA

Marketing start

2012-10-04

Marketing end

0000-00-00

Substance

CEFUROXIME SODIUM

Active strength

2 g/16mL

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record