# Cyclobenzaprine Hydrochloride

NDC: 72603-312
Generic name: Cyclobenzaprine Hydrochloride
Labeler / Manufacturer: NORTHSTAR RX LLC
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: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72603-312"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-312
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2a3a13c3-116c-4e9e-a7f3-7ad7c80486c3