Linezolid

Product NDC

70518-0527

11-digit product format

705180527

Labeler code

70518

Product ID

70518-0527_85968b39-257c-6104-e053-2991aa0a328d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Linezolid

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA204239

Marketing category

ANDA

Marketing start

2017-05-12

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

2020-12-31

Current FDA listing

Historical FDA.report record