United States · FDA National Drug Code directory
TRYVIO
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
- 80491-8012_44bb9bce-c692-4295-805a-14aed0e7fb04
- Product NDC
- 80491-8012
- Form
- TABLET, FILM COATED
- Composition / generic term
- Aprocitentan
- Labeler
- Idorsia Pharmaceuticals Ltd
- Marketing category
- NDA
- Marketing start / end (source format)
- 20240320
- Source listing expiry
- 20271231
Source-listed ingredients
- APROCITENTAN — 12.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (80491-8012-3) / 30 TABLET, FILM COATED in 1 BOTTLE · 80491-8012-3
- 1 BLISTER PACK in 1 CARTON (80491-8012-8) / 10 TABLET, FILM COATED in 1 BLISTER PACK (80491-8012-7) · 80491-8012-8
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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