Cefazolin

Product NDC

60505-0749

11-digit product format

605050749

Labeler code

60505

Product ID

60505-0749_e93a8cbf-ede9-46e4-901b-7be2ad84d8da

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

CEFAZOLIN

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Apotex Corporation

Application

ANDA065226

Marketing category

ANDA

Marketing start

2005-10-07

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