# Ondansetron

NDC: 72572-520
Generic name: Ondansetron
Labeler / Manufacturer: Civica, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20191118

FDA application: ANDA077541

## Active ingredients

- ONDANSETRON HYDROCHLORIDE: 2 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72572-520"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72572-520
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=70437694-0341-4f3b-824c-06843403443f