# ONDANSETRON

NDC: 76045-216
Generic name: ONDANSETRON HYDROCHLORIDE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20220531

FDA application: ANDA202253

## Active ingredients

- ONDANSETRON HYDROCHLORIDE: 4 mg/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76045-216"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76045-216
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d89017aa-b8c3-4fd2-8e68-44e2cfd6f290