# ondansetron hydrochloride

NDC: 83980-017
Generic name: ondansetron hydrochloride
Labeler / Manufacturer: Ipca Laboratories Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260814

FDA application: ANDA203761

## Active ingredients

- ONDANSETRON HYDROCHLORIDE: 4 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"83980-017"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83980-017
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7ab3210e-eed1-479a-afc0-f72b5b776883