# Doxepin

NDC: 0228-3316
Generic name: Doxepin
Labeler / Manufacturer: Actavis Pharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200102

FDA application: ANDA201951

## Active ingredients

- DOXEPIN HYDROCHLORIDE: 6 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0228-3316"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0228-3316
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c42333f8-1add-4f33-9458-6fe4436874a1