CEFAZOLIN

Product NDC

55154-9559

11-digit product format

551549559

Labeler code

55154

Product ID

55154-9559_acd456a9-3bb0-4e53-83fc-76c704ca1cb8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

CEFAZOLIN SODIUM

Dosage form

POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Cardinal Health

Application

ANDA065303

Marketing category

ANDA

Marketing start

2011-07-15

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