MAXIPIME

Product NDC

0409-0219

11-digit product format

004090219

Labeler code

0409

Product ID

0409-0219_51b99895-f949-4994-a762-e79ac6a322fb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefepime

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Hospira, Inc.

Application

NDA050679

Marketing category

NDA

Marketing start

2013-02-18

Marketing end

0000-00-00

Substance

CEFEPIME HYDROCHLORIDE

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