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
- 55111-154_b5be4b6c-42cd-c9b3-a0df-e15c946ec89b
- Product NDC
- 55111-154
- Form
- TABLET, FILM COATED
- Composition / generic term
- ONDANSETRON HYDROCHLORIDE
- Labeler
- Dr. Reddy's Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20061226
- Source listing expiry
- 20261231
Source-listed ingredients
- ONDANSETRON HYDROCHLORIDE — 8 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (55111-154-01) · 55111-154-01
- 500 TABLET, FILM COATED in 1 BOTTLE (55111-154-05) · 55111-154-05
- 3 DOSE PACK in 1 BOX (55111-154-13) / 1 TABLET, FILM COATED in 1 DOSE PACK · 55111-154-13
- 30 TABLET, FILM COATED in 1 BOTTLE (55111-154-30) · 55111-154-30
- 10 DOSE PACK in 1 BOX (55111-154-78) / 10 TABLET, FILM COATED in 1 DOSE PACK (55111-154-79) · 55111-154-78
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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