# Doxepin

NDC: 72162-2474
Generic name: doxepin hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220912

FDA application: ANDA202510

## Active ingredients

- DOXEPIN HYDROCHLORIDE: 3 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-2474"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-2474
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bc3b0401-df4a-46a2-a29b-3d70e72aa88b