# Paliperidone

NDC: 65162-281
Generic name: Paliperidone
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20190924

FDA application: ANDA204707

## 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:"65162-281"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65162-281
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7b269778-803b-4ce2-a8c0-636fb131d16a