# Cyclobenzaprine Hydrochloride

NDC: 80425-0019
Generic name: Cyclobenzaprine Hydrochloride
Labeler / Manufacturer: Advanced Rx of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20170330

FDA application: ANDA077797

## Active ingredients

- CYCLOBENZAPRINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0019"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0019
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=afcad582-ab59-4f70-e053-2a95a90a04e4