# CYCLOBENZAPRINE HYDROCHLORIDE

NDC: 42708-197
Generic name: cyclobenzaprine hydrochloride
Labeler / Manufacturer: QPharma, Inc.
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

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42708-197"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42708-197
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4dcbdf8f-37ce-0f90-e063-6394a90ae83c