Ceftriaxone Sodium

Product NDC

68071-1829

11-digit product format

680711829

Labeler code

68071

Product ID

68071-1829_59283950-c217-da1f-e053-2991aa0ac82a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ceftriaxone Sodium

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

NuCare Pharmceuticals,Inc.

Application

ANDA065169

Marketing category

ANDA

Marketing start

2005-05-09

Marketing end

0000-00-00

Substance

CEFTRIAXONE SODIUM

Active strength

250 mg/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