CEFTRIAXONE

Product NDC

50090-1773

11-digit product format

500901773

Labeler code

50090

Product ID

50090-1773_c1811c6a-d803-42b9-86ec-94de86e3c082

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

CEFTRIAXONE

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

A-S Medication Solutions

Application

ANDA065125

Marketing category

ANDA

Marketing start

2009-06-01

Marketing end

0000-00-00

Substance

CEFTRIAXONE SODIUM

Active strength

500 mg/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