Wednesday, July 8, 2026

Drug profile · INN

florbetapir f-18

florbetapir f-18 (AMYVID) is a diagnostic agent. Route of administration: intravenous. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 5
News articles 0
Drug details — florbetapir f-18
US status
approved
Class
Route
INTRAVENOUS
Patents
0
Programs
5
Data quality
0.84

Quick answer

florbetapir f-18 (AMYVID) is a diagnostic agent. Route of administration: intravenous. Current US regulatory status: approved.

Key facts

INN florbetapir f-18
Brand AMYVID
Mechanism Diagnostic agent
Route INTRAVENOUS
Formulation SOLUTION

Mechanism of action

Diagnostic agent

Approval history

Authority Status Date
FDA approved

Pipeline programs

  1. WN45443 Phase 3 · HOFFMANN-LA ROCHE · Early Symptomatic Alzheimer’s Disease (MCI to Mild Dementia
  2. WN45447 Phase 3 · HOFFMANN-LA ROCHE · Early Symptomatic Alzheimer’s Disease (MCI to Mild Dementia
  3. 219867 Phase 2 · GSK Glaxo Smith · Alzheimer's Disease
  4. ACU193-201 Phase 2 · Acumen Pharmaceuticals · Early Alzheimer’s Disease (Mild Cognitive Impairment and Mi
  5. Florbetapir F 18 (18F-AV-45) Approved · BRIGHT MINDS BIOSCIENCES · Postoperative Cognitive Dysfunction

Frequently asked questions

What is florbetapir f-18?

florbetapir f-18 (AMYVID) is a diagnostic agent. Route of administration: intravenous. Current US regulatory status: approved.

What is the brand name for florbetapir f-18?

AMYVID is a marketed brand name for florbetapir f-18. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of florbetapir f-18?

florbetapir f-18 has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.