Cefazolin

Product NDC

55154-6668

11-digit product format

551546668

Labeler code

55154

Product ID

55154-6668_d676bded-3872-44c7-b4b2-c618d5be91c7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefazolin

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Cardinal Health

Application

ANDA065226

Marketing category

ANDA

Marketing start

2012-04-20

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