CEFOTAXIME

Product NDC

68180-811

11-digit product format

681800811

Labeler code

68180

Product ID

68180-811_b5024702-310b-4170-a820-86ba597c4894

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

CEFOTAXIME

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Lupin Pharmaceuticals, Inc.

Application

ANDA065124

Marketing category

ANDA

Marketing start

2005-05-27

Marketing end

0000-00-00

Substance

CEFOTAXIME SODIUM

Active strength

500 mg/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