Ceftriaxone

Product NDC

70518-0384

11-digit product format

705180384

Labeler code

70518

Product ID

70518-0384_4c7412be-2fa1-40a2-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ceftriaxone

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

REMEDYREPACK INC.

Application

ANDA065342

Marketing category

ANDA

Marketing start

2017-04-03

Marketing end

0000-00-00

Substance

CEFTRIAXONE SODIUM

Active strength

1 g/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record