# Trazodone Hydrochloride

NDC: 70518-1204
Generic name: Trazodone Hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180515
Marketing ended: 20281231
FDA application: ANDA205253

## 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:"70518-1204"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-1204
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0545507a-5c11-4451-872a-d2f7f0aaecd4