# Paroxetine Hydrochloride

NDC: 62175-472
Generic name: Paroxetine Hydrochloride
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20141031

FDA application: ANDA204744

## Active ingredients

- PAROXETINE HYDROCHLORIDE: 37.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62175-472"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62175-472
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f22886f5-230c-47e4-9dd8-ffb14c8d6ae4