Cefazolin

Product NDC

60505-0769

11-digit product format

605050769

Labeler code

60505

Product ID

60505-0769_d41f90f4-1248-4e64-8b53-b78574024e16

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefazolin

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Apotex Corporation

Application

ANDA065247

Marketing category

ANDA

Marketing start

2006-06-13

Marketing end

0000-00-00

Substance

CEFAZOLIN SODIUM

Active strength

10 g/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record