Linezolid

Product NDC

60687-189

11-digit product format

606870189

Labeler code

60687

Product ID

60687-189_659192be-a56b-8557-e053-2991aa0ac847

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Linezolid

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

American Health Packaging

Application

ANDA205517

Marketing category

ANDA

Marketing start

2016-02-10

Marketing end

2019-04-30

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