# Doxepin Hydrochloride

NDC: 54838-512
Generic name: Doxepin Hydrochloride
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 19981229

FDA application: ANDA074721

## Active ingredients

- DOXEPIN HYDROCHLORIDE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"54838-512"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=54838-512
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f350afed-120b-422d-9e6e-3aaa0f72a5fb