Cefazolin

Product NDC

50090-2714

11-digit product format

500902714

Labeler code

50090

Product ID

50090-2714_e2aff5dc-4157-4de0-abfb-86e5beb6f85f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

CEFAZOLIN

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

A-S Medication Solutions

Application

ANDA065226

Marketing category

ANDA

Marketing start

2009-03-27

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