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
60760-936_57e8a220-b3c9-f7c8-e063-6294a90a0931
Product NDC
60760-936
Form
TABLET, ORALLY DISINTEGRATING
Composition / generic term
Ondansetron
Labeler
St. Mary's Medical Park Pharmacy
Marketing category
ANDA
Marketing start / end (source format)
20251015
Source listing expiry
20271231

Source-listed ingredients

  • ONDANSETRON — 8 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (60760-936-10) · 60760-936-10

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.

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