Cefazolin

Product NDC

55154-7463

11-digit product format

551547463

Labeler code

55154

Product ID

55154-7463_6ad3f907-51f9-4e46-aa29-a2c6891d1208

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefazolin

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Cardinal Health

Application

ANDA065047

Marketing category

ANDA

Marketing start

2001-09-18

Marketing end

2019-07-31

Substance

CEFAZOLIN SODIUM

Active strength

330 mg/mL

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record