# Cyclobenzaprine Hydrochloride

NDC: 72189-545
Generic name: Cyclobenzaprine Hydrochloride
Labeler / Manufacturer: Direct_Rx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240409

FDA application: ANDA208170

## 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:"72189-545"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-545
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=15aad4af-5c05-be36-e063-6294a90a9bb3