MAXIPIME

Product NDC

0409-0220

11-digit product format

004090220

Labeler code

0409

Product ID

0409-0220_66282ed1-7f59-4e18-bff9-34f619f1682b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefepime

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Hospira, Inc.

Application

NDA050679

Marketing category

NDA

Marketing start

2013-02-18

Marketing end

2020-01-31

Substance

CEFEPIME HYDROCHLORIDE

Active strength

2 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