# Trazodone Hydrochloride

NDC: 68788-7166
Generic name: Trazodone Hydrochloride
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180605

FDA application: ANDA205253

## Active ingredients

- TRAZODONE HYDROCHLORIDE: 150 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-7166"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-7166
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bb3ecde6-72ca-450c-ba88-9cf45c808d90