Metaxalone

Product NDC
55700-342
11-digit product format
557000342
Labeler code
55700
Product ID
55700-342_438d2ae3-4dc2-4367-8858-0550424d2ed8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metaxalone
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA203399
Marketing category
ANDA
Marketing start
2013-05-31
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

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
1NMA9J598YMETAXALONE1665-48-1METAXALONE