# Doxepin Hydrochloride

NDC: 42806-532
Generic name: Doxepin Hydrochloride
Labeler / Manufacturer: Epic Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20220303

FDA application: ANDA210675

## Active ingredients

- DOXEPIN HYDROCHLORIDE: 75 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42806-532"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42806-532
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5f0f6fee-2497-4915-b58b-bf369efcfd79