# Clozapine

NDC: 59651-263
Generic name: Clozapine
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20241212

FDA application: ANDA212923

## Active ingredients

- CLOZAPINE: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59651-263"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-263
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=caf2d4a6-2a23-4992-a807-560c4204afc4