01 1Astellas Pharma Europe Bv
02 2BIOGEN IDEC LTD
03 2Bayer AG
04 5Bayer Ag
05 2Bayer Pharma Ag
06 1Biocidal Or
07 4Biogen Netherlands B.V.
08 4Biogen Netherlands BV
09 19Biogen Netherlands Bv
10 3Biogen Switzerland Ag
11 7MERCK SERONO EUROPE LTD
12 11Merck (Switzerland) Ag
13 26Merck Europe B.V.
14 11Merck Europe Bv
15 2Novartis Europharm Limited
16 1Orifarm AS
17 4Serono Europe Ltd.
01 9INTERFERON BETA-1A
02 1Interferon Alfacon-1
03 30Interferon Beta-1A
04 7Interferon Beta-1B
05 13Interferon Beta-1a (rDNA origin)
06 9Interferon beta
07 14Interferon beta-1a
08 3Interferon beta-1b
09 14Peginterferon Beta-1A
10 4Peginterferon beta-1a
11 1Sodium Chloride; Interferon Beta-1B
01 12Injectable Solution
02 3Injectable Solution In Cartridge
03 2Injectable Solution In Pre-Filled Pen
04 3Injectable Solution In Pre-Filled Syringe
05 3Injection Solution
06 2Interferon Beta 1A 22Mcg 12 Units Parenteral Use
07 1Interferon Beta 1A 22Mcg 4 Units Parenteral Use
08 2Interferon Beta 1A 30Mcg 4 Units Parenteral Use
09 2Interferon Beta 1A 44Mcg 12 Units Parenteral Use
10 1Interferon Beta 1A 44Mcg 4 Units Parenteral Use
11 1Interferon Beta 1A 8,8Mcg 6 Units + 22Mcg 6 Units Parenteral Use
12 6Powder And Solvent For Injectable Solution
13 65Solution For Injection
14 2Solution For Injection In Pre-Filled Pen
01 18Denmark
02 13Estonia
03 9Italy
04 3Moldova
05 14Norway
06 15Spain
07 19Sweden
08 14Switzerland
01 13Avonex
02 1Avonex Pen
03 8Betaferon
04 1Betaferon®
05 1Blastoferon®
06 1Extavia
07 1Extravia
08 1Infergen
09 17Plegridy
10 1Plegridy
11 49Rebif
12 3Rebif (HSA-haltige Formulierung)
13 2Rebif RebiDose
14 2Rebif multidose
15 1Rebif starter pack
16 1Rebif und
17 1Rebif und RebiDose
18 1Rebif®
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Infergen
Dosage Form : Injectable Solution
Dosage Strength : 9mcg
Packaging :
Approval Date : 01/02/1999
Application Number : 19990201000016
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Betaferon
Dosage Form : Solution For Injection
Dosage Strength : 250mcg/ml
Packaging :
Approval Date : 30/11/1995
Application Number : 19951130000010
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info :
Registration Country : Moldova
Brand Name : Betaferon®
Dosage Form : Solution For Injection
Dosage Strength : 250mcg/ml
Packaging :
Approval Date : 26-08-2021
Application Number :
Regulatory Info :
Registration Country : Moldova
Regulatory Info : Marketed
Registration Country : Norway
Brand Name : Betaferon
Dosage Form : Solution For Injection
Dosage Strength : 250mcg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
Regulatory Info : Not Marketed
Registration Country : Norway
Brand Name : Betaferon
Dosage Form : Solution For Injection
Dosage Strength : 250mcg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Not Marketed
Registration Country : Norway
Regulatory Info : Cancelled
Registration Country : Spain
Sodium Chloride; Interferon Beta-1B
Brand Name : Betaferon
Dosage Form : Powder And Solvent For Injectable Solution
Dosage Strength : 250MCG
Packaging :
Approval Date : 05-05-2000
Application Number : 95003003
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Betaferon
Dosage Form : Powder And Solvent For Injectable Solution
Dosage Strength : 250MCG
Packaging :
Approval Date : 15-04-2008
Application Number : 95003005
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Betaferon
Dosage Form : Powder And Solvent For Injectable Solution
Dosage Strength : 250MCG
Packaging :
Approval Date : 19-12-2008
Application Number : 95003008
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Betaferon
Dosage Form : Powder And Solvent For Injectable Solution
Dosage Strength : 250MCG
Packaging :
Approval Date : 10-07-2015
Application Number : 95003005IP
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Betaferon
Dosage Form : Powder And Solvent For Injectable Solution
Dosage Strength : 250MCG
Packaging :
Approval Date : 01-10-2019
Application Number : 95003005IP1
Regulatory Info : Authorized
Registration Country : Spain
