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
- 63187-065_dcd5d6d3-2419-467f-91c2-50586e9ca5cb
- Product NDC
- 63187-065
- Form
- TABLET, FILM COATED
- Composition / generic term
- ONDANSETRON
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070625
- Source listing expiry
- 20261231
Source-listed ingredients
- ONDANSETRON HYDROCHLORIDE — 8 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET, FILM COATED in 1 BOTTLE (63187-065-10) · 63187-065-10
- 15 TABLET, FILM COATED in 1 BOTTLE (63187-065-15) · 63187-065-15
- 20 TABLET, FILM COATED in 1 BOTTLE (63187-065-20) · 63187-065-20
- 30 TABLET, FILM COATED in 1 BOTTLE (63187-065-30) · 63187-065-30
- 60 TABLET, FILM COATED in 1 BOTTLE (63187-065-60) · 63187-065-60
- 90 TABLET, FILM COATED in 1 BOTTLE (63187-065-90) · 63187-065-90
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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