# Paroxetine

NDC: 69367-337
Generic name: Paroxetine
Labeler / Manufacturer: Westminster Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20210726

FDA application: ANDA213485

## Active ingredients

- PAROXETINE HYDROCHLORIDE: 37.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69367-337"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69367-337
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f39a2a7a-7a7e-4dd8-9704-54d9598504fb