# CHLORZOXAZONE

NDC: 16571-725
Generic name: CHLORZOXAZONE
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220405

FDA application: ANDA213126

## Active ingredients

- CHLORZOXAZONE: 375 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16571-725"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-725
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1df6058b-7bf2-4246-9827-93fa023a5fd4