# Paroxetine

NDC: 68071-2835
Generic name: paroxetine hydrochloride hemihydrate
Labeler / Manufacturer: NuCare Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220329

FDA application: ANDA203854

## Active ingredients

- PAROXETINE HYDROCHLORIDE HEMIHYDRATE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-2835"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-2835
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=49dd0858-685f-f46b-e063-6294a90a7f39