# Cyclobenzaprine Hydrochloride

NDC: 59746-177
Generic name: Cyclobenzaprine Hydrochloride
Labeler / Manufacturer: Jubilant Cadista Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20060404

FDA application: ANDA077563

## Active ingredients

- CYCLOBENZAPRINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59746-177"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59746-177
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=592871f6-0eb2-4624-9e10-bd8bf767c002