# Trazodone Hydrochloride

NDC: 50111-561
Generic name: Trazodone Hydrochloride
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20201008

FDA application: ANDA071524

## Active ingredients

- TRAZODONE HYDROCHLORIDE: 100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50111-561"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50111-561
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4006d439-e2de-4590-82e9-fc9d56e3ec1b