# Paroxetine

NDC: 65841-601
Generic name: Paroxetine Hydrochloride
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20070413

FDA application: ANDA077584

## Active ingredients

- PAROXETINE HYDROCHLORIDE ANHYDROUS: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65841-601"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65841-601
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6d5fcdb2-4d84-4b20-87e3-58a43e567500