Ceftriaxone Sodium

Product NDC

0781-9329

11-digit product format

007819329

Labeler code

0781

Product ID

0781-9329_d9662c76-643a-4330-b7c9-9a6c46574dca

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ceftriaxone Sodium

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Sandoz Inc

Application

ANDA065169

Marketing category

ANDA

Marketing start

2005-05-09

Marketing end

0000-00-00

Substance

CEFTRIAXONE SODIUM

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