Cefazolin

Product NDC

0409-0806

11-digit product format

004090806

Labeler code

0409

Product ID

0409-0806_ae5e8eb1-b286-4b1b-804b-9791ed2d5962

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefazolin

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Hospira, Inc.

Application

ANDA065247

Marketing category

ANDA

Marketing start

2009-03-27

Marketing end

0000-00-00

Substance

CEFAZOLIN SODIUM

Active strength

10 g/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record