# Doxepin hydrochloride

NDC: 70518-3594
Generic name: Doxepin hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20221213

FDA application: ANDA212624

## Active ingredients

- DOXEPIN HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-3594"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-3594
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4ecd3b43-b5f1-4cf4-af36-eb214c1a3c60