# ziprasidone hydrochloride

NDC: 70518-2294
Generic name: ziprasidone hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20190903

FDA application: ANDA077565

## Active ingredients

- ZIPRASIDONE HYDROCHLORIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-2294"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-2294
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7e7261d7-4902-4bb5-a268-6c358890f963