United States · FDA National Drug Code directory
ONDANSETRON
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 61919-565_4b32211f-c9b5-5ea2-e063-6394a90a2834
- Product NDC
- 61919-565
- Form
- TABLET, FILM COATED
- Composition / generic term
- ONDANSETRON
- Labeler
- Direct_Rx
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190822
- Source listing expiry
- 20271231
Source-listed ingredients
- ONDANSETRON HYDROCHLORIDE — 4 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (61919-565-30) · 61919-565-30
- 45 TABLET, FILM COATED in 1 BOTTLE (61919-565-45) · 61919-565-45
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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