# Ondansetron Hydrochloride

NDC: 0054-0064
Generic name: Ondansetron Hydrochloride
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20061226

FDA application: ANDA076960

## Active ingredients

- ONDANSETRON HYDROCHLORIDE: 4 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0054-0064"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0054-0064
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1a0c4dc6-643e-4ee7-92a9-edb98049a5ba