Cefazolin

Product NDC

52584-024

11-digit product format

525840024

Labeler code

52584

Product ID

52584-024_15d3eeb9-822a-4035-a227-601e4f66b380

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefazolin

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

General Injectables & Vaccines, Inc

Application

ANDA062831

Marketing category

ANDA

Marketing start

2012-04-12

Marketing end

0000-00-00

Substance

CEFAZOLIN SODIUM

Active strength

500 mg/500mg

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record