# Cyclobenzaprine Hydrochloride

NDC: 50268-190
Generic name: Cyclobenzaprine Hydrochloride
Labeler / Manufacturer: AvPAK
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20140610

FDA application: ANDA090478

## Active ingredients

- CYCLOBENZAPRINE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50268-190"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50268-190
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=64f6d1be-4067-a5c7-2343-4aed651a0cac