Ceftazidime

Product NDC

0781-3178

11-digit product format

007813178

Labeler code

0781

Product ID

0781-3178_f855e6f8-527b-4534-94f8-a97ceafdaa31

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ceftazidime

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Sandoz Inc

Application

ANDA062640

Marketing category

ANDA

Marketing start

2008-05-15

Marketing end

0000-00-00

Substance

CEFTAZIDIME

Active strength

2 g/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record