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Coagulation Factors

Coagulation factors are protein components of the blood which serve blood coagulation.

Search results 26 to 50 from a total of 90

Name Mar­ket­ing Au­tho­ri­sa­tion Hold­er Li­cense Num­ber Li­cense Date Further Information

Fanhdi 1000 I.E.

Grifols Deutschland GmbH

10565a/97-3 12.08.1999

Fanhdi 250 I.E.

Grifols Deutschland GmbH

10565a/97-1 12.08.1999

Fanhdi 500 I.E.

Grifols Deutschland GmbH

10565a/97-2 12.08.1999

OCTANINE F 500

OCTAPHARMA GmbH

10501a/97-2 07.09.2000

OCTANINE F 1000

OCTAPHARMA GmbH

10501a/97-3 07.09.2000

OCTAPLEX 500

OCTAPHARMA GmbH

PEI.H.02312.01.1 14.03.2003

ADVATE

Takeda Manufacturing Austria AG

EU/1/03/271 02.03.2004

EPAR ADVATE

Fibrogammin 1250

CLS Behring GmbH

PEI.H.03242.02.1 07.02.2005

Fibrogammin 250

CSL Behring GmbH

PEI.H.03242.01.1 07.02.2005

Wilate 450

OCTAPHARMA GmbH

PEI.H.01918.01.1 08.02.2005

Wilate 900

OCTAPHARMA GmbH

PEI.H.01918.02.1 08.02.2005

Haemocomplettan P 2g

CSL Behring GmbH

PEI.H.03265.02.1 22.03.2005 Rote-Hand-Brief: Haemocomplettan und Riastap (01.04.2019)

Haemocomplettan P 1g

CSL Behring GmbH

PEI.H.03265.01.1 22.03.2005 Rote-Hand-Brief: Haemocomplettan und Riastap (01.04.2019)

Immuseven

Takeda GmbH

PEI.H.03341.01.1 28.11.2005

Fanhdi 1500 I.E.

Grifols Deutschland GmbH

PEI.H.03436.01.1 24.08.2006

Cofact 500

Prothya Biosolutions Netherlands B.V.

PEI.H.03453.02.1 31.08.2007

IMMUNINE 1200 I.E.

Takeda GmbH

PEI.H.03595.03.1 05.05.2008

IMMUNINE 600 I.E.

Takeda GmbH

PEI.H.03595.02.1 05.05.2008

Haemonine 1000

Biotest Pharma GmbH

PEI.H.03626.03.1 02.01.2009

Haemonine 500

Biotest Pharma GmbH

PEI.H.03626.02.1 02.01.2009

WILLFACT 1000 I.E.

LFB-Biomedicaments

PEI.H.03530.01.1 15.05.2009

Riastap 1 g

CSL Behring GmbH

PEI.H.04771.01.1 03.12.2009 Rote-Hand-Brief: Haemocomplettan und Riastap (01.04.2019)

Wilate 500

OCTAPHARMA GmbH

PEI.H.01918.03.1 22.12.2011

Wilate 1000

OCTAPHARMA GmbH

PEI.H.01918.04.1 22.12.2011

NovoThirteen

Novo Nordisk A/S, Denmark

EU/1/12/775 03.09.2012

EPAR: NovoThirteen

Disclaimer

The list of medicines contains the products that have a valid marketing authorization. It contains no information as to whether the preparations are available on the market.

The information contained in the Federal Gazette, which is the official publication organ of the Paul-Ehrlich-Institut, is legally binding.

As of: PEI announcement No. 520 in BAnz AT 22.08.2024 B6.

Summary of Product Characteristics (SmPCs) and the Package Leaflet (PL)

Where the European Medicines Agency (EMA) offers further information, you will find a link to the EPAR (European public assessment report) in the table.

If user and technical information or public assessment reports are available in PharmNet.Bund, the Federal and State Pharmaceutical Information Portal, these are directly linked to PharmNet.Bund in the table.

Updated: 22.08.2024