# Ondansetron Hydrochloride

NDC: 68999-555
Generic name: Ondansetron Hydrochloride
Labeler / Manufacturer: Chartwell Governmental & Specialty RX, LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20110127

FDA application: ANDA091342

## Active ingredients

- ONDANSETRON HYDROCHLORIDE: 4 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68999-555"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68999-555
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7e862601-1d8a-455b-8ce5-1a32478b309f