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 UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 1NMA9J598Y | METAXALONE | 1665-48-1 | METAXALONE |