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
- 51407-004_49684d71-7db8-3561-e063-6394a90a2def
- Product NDC
- 51407-004
- Form
- TABLET
- Composition / generic term
- Ondansetron
- Labeler
- Golden State Medical Supply, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070625
- Source listing expiry
- 20271231
Source-listed ingredients
- ONDANSETRON HYDROCHLORIDE — 8 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET in 1 BOTTLE (51407-004-05) · 51407-004-05
- 30 TABLET in 1 BOTTLE (51407-004-30) · 51407-004-30
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →