# paroxetine hydrochloride

NDC: 69584-673
Generic name: paroxetine hydrochloride
Labeler / Manufacturer: Oxford Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20221114

FDA application: ANDA076968

## Active ingredients

- PAROXETINE HYDROCHLORIDE: 30 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69584-673"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69584-673
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=25182b68-8f7a-48e8-9788-6818b0984b29