# Trazodone Hydrochloride

NDC: 70010-232
Generic name: Trazodone Hydrochloride
Labeler / Manufacturer: Granules Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240809

FDA application: ANDA218988

## 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:"70010-232"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70010-232
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5bc5f266-6c0e-4b9a-b6e0-ea694928b948