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
- 83980-012_3582cf26-d9a0-4b93-93a1-d1824e55fc19
- Product NDC
- 83980-012
- Form
- TABLET, ORALLY DISINTEGRATING
- Composition / generic term
- Ondansetron
- Labeler
- Ipca Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250619
- Source listing expiry
- 20261231
Source-listed ingredients
- ONDANSETRON — 4 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (83980-012-01) · 83980-012-01
- 1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (83980-012-10) · 83980-012-10
- 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (83980-012-13) · 83980-012-13
- 3 BLISTER PACK in 1 CARTON (83980-012-83) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK · 83980-012-83
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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