LINEZOLID

Product NDC

0093-8244

11-digit product format

000938244

Labeler code

0093

Product ID

0093-8244_901ed105-f874-47e7-83c1-f7d649b926f9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Linezolid

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Teva Pharmaceuticals USA Inc

Application

NDA021130

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2015-06-22

Marketing end

0000-00-00

Substance

LINEZOLID

Active strength

600 mg/1

Pharmacologic classes

Oxazolidinone Antibacterial [EPC],Oxazolidinones [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record