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
- 71205-744_33d02d85-fb3b-48c1-85db-4be993bfcc96
- Product NDC
- 71205-744
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ondansetron Hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070731
- Source listing expiry
- 20261231
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 (71205-744-10) · 71205-744-10
- 12 TABLET, FILM COATED in 1 BOTTLE (71205-744-12) · 71205-744-12
- 15 TABLET, FILM COATED in 1 BOTTLE (71205-744-15) · 71205-744-15
- 20 TABLET, FILM COATED in 1 BOTTLE (71205-744-20) · 71205-744-20
- 30 TABLET, FILM COATED in 1 BOTTLE (71205-744-30) · 71205-744-30
- 60 TABLET, FILM COATED in 1 BOTTLE (71205-744-60) · 71205-744-60
- 90 TABLET, FILM COATED in 1 BOTTLE (71205-744-90) · 71205-744-90
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →