# Doxepin Hydrochloride

NDC: 71921-166
Generic name: Doxepin Hydrochloride
Labeler / Manufacturer: Florida Pharmaceutical Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210501

FDA application: ANDA213474

## Active ingredients

- DOXEPIN HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71921-166"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71921-166
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b787a283-f882-e1f0-e053-2a95a90a8975