# Doxepin

NDC: 72603-222
Generic name: Doxepin
Labeler / Manufacturer: North Star Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240401

FDA application: ANDA202337

## 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:"72603-222"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-222
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=12edd5c6-c863-b83a-e063-6294a90a2f36