Metaxalone

Product NDC

50436-0448

11-digit product format

504360448

Labeler code

50436

Product ID

50436-0448_d42eb6ce-d25c-40df-b98f-72d9e916a577

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metaxalone

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA040445

Marketing category

ANDA

Marketing start

2010-03-31

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