# PAROXETINE

NDC: 68180-647
Generic name: PAROXETINE
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20170306

FDA application: ANDA204134

## Active ingredients

- PAROXETINE HYDROCHLORIDE HEMIHYDRATE: 12.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68180-647"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-647
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d315e0da-f829-408b-be5d-2bca2e06913c