# Risperidone

NDC: 69367-372
Generic name: Risperidone
Labeler / Manufacturer: Westminster Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240909

FDA application: ANDA078707

## Active ingredients

- RISPERIDONE: 3 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69367-372"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69367-372
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=07d43bf6-a695-453a-a5c7-9581effe585c