# Chlorzoxazone

NDC: 51862-339
Generic name: chlorzoxazone
Labeler / Manufacturer: Mayne Pharma Commercial LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200731

FDA application: ANDA211849

## Active ingredients

- CHLORZOXAZONE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51862-339"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51862-339
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5238c99e-d36e-4376-ab05-ca2535213d58