LINEZOLID

Product NDC

60505-4362

11-digit product format

605054362

Labeler code

60505

Product ID

60505-4362_6a9ae370-c3e8-4e72-9cfd-11db4e27931a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Linezolid

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Apotex Corp.

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