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
- 83980-018_57713a3e-638c-494d-965e-2399c69dd00f
- Product NDC
- 83980-018
- Form
- TABLET, FILM COATED
- Composition / generic term
- ondansetron hydrochloride
- Labeler
- Ipca Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260814
- Source listing expiry
- 20271231
Source-listed ingredients
- ONDANSETRON HYDROCHLORIDE — 8 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, FILM COATED in 1 BOTTLE (83980-018-10) · 83980-018-10
- 30 TABLET, FILM COATED in 1 BOTTLE (83980-018-13) · 83980-018-13
- 10 TABLET, FILM COATED in 1 BOTTLE (83980-018-97) · 83980-018-97
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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