# Cyclobenzaprine Hydrochloride

NDC: 69097-845
Generic name: Cyclobenzaprine
Labeler / Manufacturer: Cipla USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160722

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:"69097-845"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69097-845
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=575a31fb-04c5-4001-88a7-c33adbacc6a8