Linezolid

Product NDC

0378-7077

11-digit product format

003787077

Labeler code

0378

Product ID

0378-7077_521246a6-4afc-45f1-9c76-e7c932978bee

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

linezolid

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Pharmaceuticals Inc.

Application

ANDA078845

Marketing category

ANDA

Marketing start

2015-12-21

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