# DOXEPIN HYDROCHLORIDE

NDC: 69315-159
Generic name: DOXEPIN HYDROCHLORIDE
Labeler / Manufacturer: Leading Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210415

FDA application: ANDA211619

## Active ingredients

- DOXEPIN HYDROCHLORIDE: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69315-159"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69315-159
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e6a4cb10-1928-4abe-8797-404c9ddc37dd