Wednesday, July 8, 2026

Drug profile · INN

eptifibatide

eptifibatide (EPTIFIBATIDE ACCORD) is a integrin alpha-iib/beta-3 inhibitor. Associated with Teva Pharma GmbH. Route of administration: injection. Current US regulatory status: approved.

FDA: approved EMA: approved Blood and blood forming organs (B01) B01AC16
US status approved
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Drug details — eptifibatide
US status
approved
Class
Blood and blood forming organs (B01)
Route
INJECTION
Patents
0
Programs
0
Data quality
0.89

Quick answer

eptifibatide (EPTIFIBATIDE ACCORD) is a integrin alpha-iib/beta-3 inhibitor. Associated with Teva Pharma GmbH. Route of administration: injection. Current US regulatory status: approved.

Key facts

INN eptifibatide
Brand EPTIFIBATIDE ACCORD
Mechanism Integrin alpha-IIb/beta-3 inhibitor
Target Integrin alpha-IIb/beta-3
Therapeutic class Blood and blood forming organs (B01)
Route INJECTION
Formulation INJECTABLE
ATC code B01AC16

Mechanism of action

Integrin alpha-IIb/beta-3 inhibitor

Primary target: Integrin alpha-IIb/beta-3

Approval history

Authority Status Date
FDA approved
EMA approved

Related & competitor drugs

  1. apixaban Blood and blood forming organs (B01)
  2. berotralstat Blood and blood forming organs (B06)
  3. bivalirudin Blood and blood forming organs (B01)
  4. c1 inhibitor (human) Blood and blood forming organs (B06)
  5. clopidogrel Blood and blood forming organs (B01)
  6. dabigatran etexilate Blood and blood forming organs (B01)

Frequently asked questions

What is eptifibatide?

eptifibatide (EPTIFIBATIDE ACCORD) is a integrin alpha-iib/beta-3 inhibitor. Associated with Teva Pharma GmbH. Route of administration: injection. Current US regulatory status: approved.

What is the brand name for eptifibatide?

EPTIFIBATIDE ACCORD is a marketed brand name for eptifibatide. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of eptifibatide?

eptifibatide 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.