# Doxepin hydrochloride

NDC: 72205-052
Generic name: Doxepin hydrochloride
Labeler / Manufacturer: Novadoz Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230405

FDA application: ANDA214823

## Active ingredients

- DOXEPIN HYDROCHLORIDE: 3 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72205-052"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72205-052
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=96086fd8-8fa3-4a2b-ac12-fe1a3ad4f384