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
- 63187-636_2996955e-2b6c-4702-8c4a-6ab17c9e6e87
- Product NDC
- 63187-636
- 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 — 4 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TABLET, FILM COATED in 1 BOTTLE (63187-636-01) · 63187-636-01
- 3 TABLET, FILM COATED in 1 BOTTLE (63187-636-03) · 63187-636-03
- 6 TABLET, FILM COATED in 1 BOTTLE (63187-636-06) · 63187-636-06
- 10 BLISTER PACK in 1 CARTON (63187-636-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 63187-636-10
- 12 TABLET, FILM COATED in 1 BOTTLE (63187-636-12) · 63187-636-12
- 15 TABLET, FILM COATED in 1 BOTTLE (63187-636-15) · 63187-636-15
- 20 TABLET, FILM COATED in 1 BOTTLE (63187-636-20) · 63187-636-20
- 30 TABLET, FILM COATED in 1 BOTTLE (63187-636-30) · 63187-636-30
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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