# Ziprasidone Hydrochloride

NDC: 65862-704
Generic name: Ziprasidone Hydrochloride
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20161227

FDA application: ANDA204117

## Active ingredients

- ZIPRASIDONE HYDROCHLORIDE: 60 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65862-704"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-704
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cc5e1c44-79e9-45d3-b1e5-b003f550c508