# Paroxetine

NDC: 72241-030
Generic name: Paroxetine
Labeler / Manufacturer: Modavar Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20211020

FDA application: ANDA212645

## Active ingredients

- PAROXETINE HYDROCHLORIDE HEMIHYDRATE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72241-030"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72241-030
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=555cfa31-3865-450f-b16b-2f4004af7a67