# PAROXETINE

NDC: 67544-317
Generic name: paroxetine hydrochloride
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20030908

FDA application: ANDA075356

## Active ingredients

- PAROXETINE HYDROCHLORIDE ANHYDROUS: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67544-317"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67544-317
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1801246b-02c3-430f-932a-b18cb0d13d1d