# Ondansetron Hydrochloride

NDC: 68094-763
Generic name: Ondansetron Hydrochloride
Labeler / Manufacturer: Precision Dose Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20150227

FDA application: ANDA076960

## 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:"68094-763"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68094-763
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=04800a86-2391-44e6-8763-d65e8a916c26