United States · FDA National Drug Code directory
Alosetron 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
- 71930-010_c304be8d-9fa3-4d89-885e-5a6bf1e80a2b
- Product NDC
- 71930-010
- Form
- TABLET
- Composition / generic term
- Alosetron Hydrochloride
- Labeler
- Eywa Pharma Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190201
- Source listing expiry
- 20261231
Source-listed ingredients
- ALOSETRON HYDROCHLORIDE — .5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71930-010-30) · 71930-010-30
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 →