United States · FDA National Drug Code directory

LOTRONEX

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
54766-894_557ed953-bb9c-8e24-e063-6394a90a525f
Product NDC
54766-894
Form
TABLET
Composition / generic term
alosetron hydrochloride
Labeler
Sebela Pharmaceuticals Inc.
Marketing category
NDA
Marketing start / end (source format)
20160711
Source listing expiry
20271231

Source-listed ingredients

  • ALOSETRON HYDROCHLORIDE — .5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (54766-894-03) · 54766-894-03

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 →