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Coagulation Factors

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

Search results 1 to 25 from a total of 89

Name Mar­ket­ing Au­tho­ri­sa­tion Hold­er Li­cense Num­ber Li­cense Date Further Information

Haemate P 500 I.E. FVIII / 1200 I.E. VWF

CSL Behring GmbH

2416.01.00 08.06.1982

Haemate P 250 I.E. FVIII / 600 I.E. VWF

CSL Behring GmbH

2416.00.00 08.06.1982

Haemate P 1000 I.E. FVIII / 2400 I.E. VWF

CSL Behring GmbH

2416.02.00 08.06.1982

IMMUNATE 500 I.E.

Takeda GmbH

3854.02.00 20.10.1983

IMMUNATE 1000 I.E.

Takeda GmbH

3854.03.00 20.10.1983

Alphanine 1000

Grifols Deutschland GmbH

6408.01.00 17.07.1985

Alphanine 500

Grifols Deutschland GmbH

6408.00.00 17.07.1985

Haemoctin SDH 500

Biotest Pharma GmbH

16841.01.00 06.11.1991

Haemoctin SDH 250

Biotest Pharma GmbH

16841.00.00 06.11.1991

Faktor VIII SDH INTERSERO 1000

Intersero GmbH

16844.02.00 06.11.1991

Haemoctin SDH 1000

Biotest Pharma GmbH

16841.02.00 06.11.1991

Faktor VIII SDH INTERSERO 250

Intersero GmbH

16844.00.00 06.11.1991

Faktor VIII SDH INTERSERO 500

Intersero GmbH

16844.01.00 06.11.1991

Recombinate Antihaemophilie Faktor (rekombinant) 1000

Takeda GmbH

28530.02.00 30.07.1993

Beriplex P/N 500

CSL Behring GmbH

10501a/95 21.02.1996

Beriplex P/N 250

CSL Behring GmbH

10500a/95 21.02.1996

NovoSeven

Novo Nordisk A/S

EU/1/96/006 23.02.1996

EPAR NovoSeven

BeneFIX

Pfizer Europe MA EEIG

EU/1/97/047 27.08.1997

EPAR BeneFIX

Beriate 250

CSL Behring GmbH

10505a/98-1 11.02.1998 Rote-Hand-Brief: Beriate (09.08.2019)

Beriate 1000

CSL Behring GmbH

10505a/98-3 11.02.1998 Rote-Hand-Brief: Beriate (09.08.2019)

Beriate 500

CSL Behring GmbH

10505a/98-2 11.02.1998 Rote-Hand-Brief: Beriate (09.08.2019)

Octanate 500

OCTAPHARMA GmbH

10500a/97-2 04.08.1998

Octanate 250

OCTAPHARMA GmbH

10500a/97-1 04.08.1998

Octanate 1000

OCTAPHARMA GmbH

10500a/97-3 04.08.1998

ReFacto AF

Pfizer Europe MA EEIG

EU/1/99/103 13.04.1999

EPAR ReFacto AF

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. 519 in BAnz AT 26.07.2024 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: 26.07.2024