# PALIPERIDONE

NDC: 31722-320
Generic name: paliperidone
Labeler / Manufacturer: Camber Pharmaceuticals, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20230823

FDA application: ANDA216174

## Active ingredients

- PALIPERIDONE: 9 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-320"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-320
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1cfcad42-da71-457d-b1e1-aee806642d0c