# Paliperidone

NDC: 69367-433
Generic name: Paliperidone
Labeler / Manufacturer: Westminster Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20251209

FDA application: ANDA218755

## Active ingredients

- PALIPERIDONE: 3 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69367-433"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69367-433
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1745a460-5e3a-4a1f-8eb3-64bb112f47a4