# Trazodone Hydrochloride

NDC: 57664-026
Generic name: Trazodone Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20221003

FDA application: ANDA073137

## Active ingredients

- TRAZODONE HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57664-026"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57664-026
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f291b905-a739-5e43-e053-2995a90ac40c