# Doxepin Hydrochloride

NDC: 72789-542
Generic name: Doxepin Hydrochloride
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20190327

FDA application: ANDA211603

## 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:"72789-542"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-542
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1496dfc1-de50-471c-be87-1f1e2b70ab5a