# DOXEPIN

NDC: 72603-920
Generic name: DOXEPIN
Labeler / Manufacturer: NorthStar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260801

FDA application: ANDA216041

## Active ingredients

- DOXEPIN HYDROCHLORIDE: 6 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72603-920"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-920
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=77782f36-d120-4c3d-bebd-c8b0f4749d98