# CYCLOBENZAPRINE HYDROCHLORIDE

NDC: 60760-766
Generic name: cyclobenzaprine hydrochloride
Labeler / Manufacturer: ST. MARY'S MEDICAL PARK PHARMACY
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20170531

FDA application: ANDA208170

## Active ingredients

- CYCLOBENZAPRINE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60760-766"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60760-766
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=00b20a8c-debd-e930-e063-6394a90a7ed0