# Doxepin hydrochloride

NDC: 64980-596
Generic name: Doxepin hydrochloride
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20231225

FDA application: ANDA217975

## 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:"64980-596"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64980-596
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=66c6af99-9909-4b18-a43b-898a1c4a34d7