# PAXIL

NDC: 60505-4518
Generic name: paroxetine hydrochloride
Labeler / Manufacturer: Apotex Corp
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190311

FDA application: NDA020031

## Active ingredients

- PAROXETINE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60505-4518"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60505-4518
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ef3b5cbe-f9e1-c1ac-79da-cfe14e3a7e7e