# Paroxetine

NDC: 62332-768
Generic name: Paroxetine
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250930

FDA application: ANDA217280

## Active ingredients

- PAROXETINE HYDROCHLORIDE HEMIHYDRATE: 37.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62332-768"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-768
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5da839f9-e2bf-4b83-a410-1226ba4552a1