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Medicines
United States
Antithrombin iii

FDA 1991

Antithrombin iii

Thrombate Iii

500IU For InjectionUnited StatesMarketedAuthorised 30 Dec 1991

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On this page

In other countries
Sources and licences

In other countries

The same active substances on other registers, the same brand first.

Thrombate IIICanada · 500 UNIT / VIAL · Powder For Solution · Grifols Therapeutics LLCSame brand
Thrombate IIICanada · 1000 UNIT / VIAL · Powder For Solution · Grifols Therapeutics LLCSame brand
Thrombate III PWS IV 1000IU/VialCanada · 1000 UNIT / VIAL · Powder For Solution · Miles INC. - Pharmaceutical DivisionSame brand
Anbinex Polvo y Disolvente Para Solucion Para PerfusionSpain · 50 UI · polvo y disolvente para solución para perfusión · Instituto Grifols S.A.Same form
Atryn 1.750 Ui Polvo Para Solucion Para PerfusionSpain · 1750 UI · polvo para solución para perfusión · Gtc Biotherapeutics Uk LimitedSame form
Antithrombin III Baxalta 50 IU/ml prašak i otapalo za otopinu za injekciju/infuzijuCroatia · Prašak i otapalo za otopinu za injekciju / infuziju · Baxalta Innovations GmbH, Industriestrasse 67, Beč, Austrija

Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

Same form

🇭🇷Kybernin P 500 prašak za otopinu za injekciju ili infuzijuCroatia · prašak i otapalo za otopinu za injekciju/infuziju · CSL Behring GmbH, Emil-von-Behring-Str. 76, Marburg, NjemačkaSame form

🇭🇷Atenativ 50 IU/ml prašak i otapalo za otopinu za injekciju/infuziju*Croatia · prašak i otapalo za otopinu za injekciju/infuziju · Jana Pharm d.o.o., Lopašićeva 6, Zagreb, HrvatskaSame form

🇮🇹AnbinexItaly · Polvere e solvente per soluzione per infusione endovenosa · Instituto Grifols S.A.Same form

🇮🇹AnternatyItaly · Polvere e solvente per soluzione per infusione endovenosa · Octapharma Italy S.P.A.Same form

🇮🇹Antitrombina III BaxaltaItaly · Polvere e solvente per soluzione per infusione endovenosa · Baxalta Innovations GMBHSame form

🇳🇱Antitrombine III concentraat Baxalta 500 IE, poeder en oplosmiddel voor injectie of intraveneuze infusieNetherlands · Poeder en oplosmiddel voor oplossing voor injectie, Poeder en oplosmiddel voor oplossing voor infusie · Baxalta Innovations GmbHSame form

🇳🇱Atenativ 50 IE/ml poeder en oplosmiddel voor oplossing voor infusieNetherlands · Poeder en oplosmiddel voor oplossing voor infusie · Octapharma GmbHSame form

🇳🇱ATenativ, poeder voor infusievloeistof 500 IE en 1000 IENetherlands · Poeder voor oplossing voor infusie · Octapharma GmbHSame form

🇷🇸Kybernin® P 500Serbia · 500i.j./10mL · prašak i rastvarač za rastvor za injekciju/infuziju · Pharmaswiss D.O.O., BeogradSame form

🇧🇷Antitrombina III GrifolsBrazil · Grifols Brasil LtdaSame substance

🇧🇷At III BaxterBrazil · Baxter Hospitalar LtdaSame substance

🇧🇷Kybernin PBrazil · CSL Behring Comércio de Produtos Farmacêuticos LtdaSame substance

🇪🇺ATrynEuropean Union · Laboratoire Francais du Fractionnement et des BiotechnologiesSame substance

🇷🇸Antitrombin III TakedaSerbia · 500i.j./10mL · prašak i rastvarač za rastvor za infuziju · Takeda DOOSame substance

🇷🇸Antitrombin III TakedaSerbia · 1000i.j./20mL · prašak i rastvarač za rastvor za infuziju · Takeda DOOSame substance

Sources and licences

Compiled by Prognia from the public register below; the register’s text is the official one.

U.S. Food and Drug Administration

FDA Purple Book, September 2026 release; acquired 2026-10-10T15:29:54.330165+00:00; exact source fields retained with source-key projections.

Licence: FDA-created structured factual administrative metadata; public-domain policy with third-party exceptions · Added 11 Oct 2026

Report an error or request removalCorrections from the holder or the register are welcome.

Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.

At a glance

Active substance: Antithrombin iii
Strength: 500IU
Dosage form: For Injection
Route: Intravenous
Register: United States (FDA)
Status: Marketed
Status in the register: Licensed / Rx
Authorised: 30 Dec 1991
Registration: BLA 103196
Marketing authorisation holder: Grifols Therapeutics LLC
Procedure: 351(a)
Supply: Rx