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
63187-379_0259eb8a-602d-42c0-a4ea-ad936de76410
Product NDC
63187-379
Form
TABLET, ORALLY DISINTEGRATING
Composition / generic term
Ondansetron
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20100412
Source listing expiry
20261231

Source-listed ingredients

  • ONDANSETRON — 4 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63187-379-03) · 63187-379-03
  • 5 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63187-379-05) · 63187-379-05
  • 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63187-379-06) · 63187-379-06
  • 7 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63187-379-07) · 63187-379-07
  • 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63187-379-10) · 63187-379-10
  • 12 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63187-379-12) · 63187-379-12
  • 15 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63187-379-15) · 63187-379-15
  • 20 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63187-379-20) · 63187-379-20
  • 30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63187-379-30) · 63187-379-30

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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