Ceftriaxone Sodium

Product NDC

68071-1828

11-digit product format

680711828

Labeler code

68071

Product ID

68071-1828_59068b37-d979-38ea-e053-2a91aa0a28c2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ceftriaxone Sodium

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA065169

Marketing category

ANDA

Marketing start

2005-05-09

Marketing end

0000-00-00

Substance

CEFTRIAXONE SODIUM

Active strength

1 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