# PAROXETINE HYDROCHLORIDE

NDC: 31722-578
Generic name: PAROXETINE HYDROCHLORIDE
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20260305

FDA application: ANDA219954

## Active ingredients

- PAROXETINE HYDROCHLORIDE: 10 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-578"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-578
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=26d37a39-1c53-461c-8834-c67fbffcfe99