Ceftriaxone Sodium

Product NDC

70518-0659

11-digit product format

705180659

Labeler code

70518

Product ID

70518-0659_89fb41de-40ae-4d22-e053-2995a90a0554

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ceftriaxone Sodium

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

REMEDYREPACK INC.

Application

ANDA065169

Marketing category

ANDA

Marketing start

2017-08-02

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