# Metaxalone

NDC: 55111-650
Generic name: Metaxalone
Labeler / Manufacturer: Dr. Reddys Laboratories Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170831

FDA application: ANDA207466

## Active ingredients

- METAXALONE: 800 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55111-650"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-650
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=02eb5938-cd59-4a81-853d-a4148d813a94