# CYCLOBENZAPRINE HYDROCHLORIDE

NDC: 76420-265
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: 20170531

FDA application: ANDA208170

## Active ingredients

- CYCLOBENZAPRINE HYDROCHLORIDE: 7.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76420-265"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-265
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2a6b2ad9-307a-4976-98b7-1b96e0408da7