# Cyclobenzaprine Hydrochloride

NDC: 82868-008
Generic name: Cyclobenzaprine Hydrochloride
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240429

FDA application: ANDA078643

## Active ingredients

- CYCLOBENZAPRINE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82868-008"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82868-008
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1912d134-a909-5511-e063-6294a90aea29