United States · FDA National Drug Code directory
Letairis
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
- 61958-0802_2808f55e-aed5-40c7-832b-630e1408951c
- Product NDC
- 61958-0802
- Form
- TABLET, FILM COATED
- Composition / generic term
- AMBRISENTAN
- Labeler
- Gilead Sciences, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20070615
- Source listing expiry
- 20271231
Source-listed ingredients
- AMBRISENTAN — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61958-0802-1) · 61958-0802-1
- 3 BLISTER PACK in 1 CARTON (61958-0802-2) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 61958-0802-2
- 1 BLISTER PACK in 1 CARTON (61958-0802-3) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 61958-0802-3
- 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61958-0802-5) · 61958-0802-5
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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