# Cyclobenzaprine Hydrochloride

NDC: 60687-558
Generic name: Cyclobenzaprine
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220210

FDA application: ANDA090478

## 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:"60687-558"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-558
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=269bc278-963d-4830-816a-39bb4bf8c936