# ONDANSETRON

NDC: 23155-549
Generic name: ONDANSETRON
Labeler / Manufacturer: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20120615

FDA application: ANDA090648

## 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:"23155-549"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-549
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b746d4db-43e6-4219-9e6b-f53e59581305