Cefazolin

Product NDC

55154-5439

11-digit product format

551545439

Labeler code

55154

Product ID

55154-5439_27eb4eae-9e38-4dbd-ad2e-4750efd57db0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefazolin

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS; PARENTERAL

Labeler

Cardinal Health

Application

ANDA062831

Marketing category

ANDA

Marketing start

1988-12-09

Marketing end

0000-00-00

Substance

CEFAZOLIN SODIUM

Active strength

1 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