Cefazolin

Product NDC

0409-0805

11-digit product format

004090805

Labeler code

0409

Product ID

0409-0805_44c28928-d498-46fd-8dde-bb7bd7255ca1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

CEFAZOLIN

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Hospira, Inc.

Application

ANDA065226

Marketing category

ANDA

Marketing start

2009-03-27

Marketing end

0000-00-00

Substance

CEFAZOLIN SODIUM

Active strength

1 g/3mL

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record