# Trazodone Hydrochloride

NDC: 69584-884
Generic name: Trazodone Hydrochloride
Labeler / Manufacturer: Oxford Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230101

FDA application: ANDA072192

## Active ingredients

- TRAZODONE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69584-884"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69584-884
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=283c8236-9776-44cb-b7b2-1024689de736