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
- 55700-627_4d8753f4-19f6-44bb-b3c2-8e5c7b98da81
- Product NDC
- 55700-627
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ondansetron Hydrochloride
- Labeler
- Quality Care Products LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180518 / 20280131
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 (55700-627-10) · 55700-627-10
- 20 TABLET, FILM COATED in 1 BOTTLE (55700-627-20) · 55700-627-20
- 30 TABLET, FILM COATED in 1 BOTTLE (55700-627-30) · 55700-627-30
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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