# PAROXETINE

NDC: 63629-9499
Generic name: PAROXETINE HYDROCHLORIDE HEMIHYDRATE
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20180914
Marketing ended: 20260731
FDA application: ANDA209293

## 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:"63629-9499"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-9499
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=51189cf4-4122-48d4-b47f-4f98a8dfb8e0