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
- 71335-0815_4633c233-c190-4611-b285-e99b5d2b7ed8
- Product NDC
- 71335-0815
- Form
- TABLET, FILM COATED
- Composition / generic term
- ondansetron hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070625
- Source listing expiry
- 20271231
Source-listed ingredients
- ONDANSETRON HYDROCHLORIDE — 8 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 TABLET, FILM COATED in 1 BOTTLE (71335-0815-0) · 71335-0815-0
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-0815-1) · 71335-0815-1
- 15 TABLET, FILM COATED in 1 BOTTLE (71335-0815-2) · 71335-0815-2
- 4 TABLET, FILM COATED in 1 BOTTLE (71335-0815-3) · 71335-0815-3
- 3 TABLET, FILM COATED in 1 BOTTLE (71335-0815-4) · 71335-0815-4
- 12 TABLET, FILM COATED in 1 BOTTLE (71335-0815-5) · 71335-0815-5
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-0815-6) · 71335-0815-6
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-0815-7) · 71335-0815-7
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-0815-8) · 71335-0815-8
- 6 TABLET, FILM COATED in 1 BOTTLE (71335-0815-9) · 71335-0815-9
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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