# Cyclobenzaprine HCL

NDC: 85509-1001
Generic name: Cyclobenzaprine HCL
Labeler / Manufacturer: PHOENIX RX LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20150325

FDA application: ANDA078722

## Active ingredients

- CYCLOBENZAPRINE HYDROCHLORIDE: 7.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"85509-1001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85509-1001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3a397e88-d267-feed-e063-6294a90a7710