Linezolid

Product NDC

0093-7490

11-digit product format

000937490

Labeler code

0093

Product ID

0093-7490_e3e2ef09-2e46-48c0-90e8-bb5bcba67cba

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Linezolid

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA078061

Marketing category

ANDA

Marketing start

2016-06-03

Marketing end

2020-05-31

Substance

LINEZOLID

Active strength

600 mg/1

Pharmacologic classes

Oxazolidinone Antibacterial [EPC],Oxazolidinones [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record