# Cyclobenzaprine Hydrochloride

NDC: 76420-599
Generic name: Cyclobenzaprine Hydrochloride
Labeler / Manufacturer: Asclemed USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20080926

FDA application: ANDA078643

## 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:"76420-599"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-599
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=74af1727-e84f-4dad-82be-045e7d23beaf