# Metaxalone

NDC: 68001-485
Generic name: Metaxalone
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210531

FDA application: ANDA207466

## Active ingredients

- METAXALONE: 800 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-485"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-485
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c91c0fb0-0b61-4e45-8bea-d0bf57ca7068