Metaxalone

Product NDC

50436-3024

11-digit product format

504363024

Labeler code

50436

Product ID

50436-3024_d65020d4-51d5-4562-967d-fab060cb1b9b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metaxalone

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

NDA013217

Marketing category

NDA

Marketing start

2007-11-01

Marketing end

0000-00-00

Substance

METAXALONE

Active strength

800 mg/1

Pharmacologic classes

Centrally-mediated Muscle Relaxation [PE]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record