# PALIPERIDONE

NDC: 43975-352
Generic name: PALIPERIDONE
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20191127

FDA application: ANDA204452

## 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:"43975-352"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43975-352
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bbbaa057-f587-4eb9-a0d2-463dbcd57661