# CYCLOBENZAPRINE HYDROCHLORIDE

NDC: 72189-101
Generic name: CYCLOBENZAPRINE HYDROCHLORIDE
Labeler / Manufacturer: DIRECT RX
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20200507

FDA application: ANDA091281

## Active ingredients

- CYCLOBENZAPRINE HYDROCHLORIDE: 15 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72189-101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a512d34c-8164-0c04-e053-2995a90a1942