# Paroxetine

NDC: 0615-8174
Generic name: Paroxetine
Labeler / Manufacturer: NCS HealthCare of KY, LLC dba Vangard Labs
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20141101

FDA application: ANDA203854

## Active ingredients

- PAROXETINE HYDROCHLORIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0615-8174"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0615-8174
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c3b2ce88-6f09-4f7b-ac73-93dca84aa3b8