# Clozapine

NDC: 0093-5377
Generic name: Clozapine
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20200730

FDA application: ANDA090308

## Active ingredients

- CLOZAPINE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-5377"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-5377
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6fccf4f7-2e30-4272-9800-225aaef20584