Inluriyo
Active substance: imlunestrant
TABLET, FILM COATED · IMLUNESTRANT 200 mg/1
United StatesActive
Marketing holder: Eli Lilly and Company
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 2
Composition
- IMLUNESTRANT · 200 mg/1
Analogues by country
Products with the same active substance registered in other countries.
| Country | Products |
|---|---|
| EU 1 |
|
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208f-9a71-7138-8ee6-b5987312e272;count=1 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 0002-1717
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 0002-1717 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 0002-1717 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 0002-1717 · Verified 2026-10-09 · open in source