United States · FDA National Drug Code directory
Ondansetron Hydrochloride
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
- 68999-555_47d4671a-9faa-ece1-e063-6394a90aaa24
- Product NDC
- 68999-555
- Form
- SOLUTION
- Composition / generic term
- Ondansetron Hydrochloride
- Labeler
- Chartwell Governmental & Specialty RX, LLC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110127
- Source listing expiry
- 20271231
Source-listed ingredients
- ONDANSETRON HYDROCHLORIDE — 4 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TRAY in 1 BOX (68999-555-24) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (68999-555-45) · 68999-555-24
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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