Linezolid

Product NDC

42292-008

11-digit product format

422920008

Labeler code

42292

Product ID

42292-008_7c75960f-5aa1-091f-e053-2991aa0af644

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

linezolid

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA078845

Marketing category

ANDA

Marketing start

2015-12-16

Marketing end

2019-05-31

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