# Doxepin Hydrochloride

NDC: 55801-528
Generic name: Doxepin Hydrochloride
Labeler / Manufacturer: Appco Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210601

FDA application: ANDA214908

## Active ingredients

- DOXEPIN HYDROCHLORIDE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55801-528"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55801-528
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=abf4c515-8888-4733-80a0-fd4e1cdb84a2