# Cyclobenzaprine Hydrochloride

NDC: 69306-075
Generic name: Cyclobenzaprine Hydrochloride
Labeler / Manufacturer: Doc Rx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20180116

FDA application: ANDA078722

## Active ingredients

- CYCLOBENZAPRINE HYDROCHLORIDE: 7.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69306-075"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69306-075
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=64669718-02a0-47c6-9709-5f8db5736e04