# Doxepin Hydrochloride

NDC: 48433-037
Generic name: doxepin hydrochloride
Labeler / Manufacturer: Safecor Health, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20260223

FDA application: ANDA070791

## Active ingredients

- DOXEPIN HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"48433-037"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=48433-037
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a2297f75-c498-419b-aa29-057271313a7f