01 4ANAKINRA
02 1AVATROMBOPAG (AVATROMBOPAG MALEATE)
03 13Anakinra
04 2Avatrombopag
05 2Avatrombopag Maleate
06 1Avatrombopagum
07 2Collagenase Clostridium Histolyticum
08 1Collagenase, Clostridium Histolyticum
09 14Efanesoctocog Alfa
10 7Efanesoctocog Alpha
11 26Efmoroctocog Alfa
12 10Eftrenonacog Alfa
13 5Eftrenonacogum Alfa
14 2Interferon Alpha (Leukocyte-derived)
15 1Loncastuximab Tesirine
16 1Lonkastuximabtesirin
17 10NITISINONE
18 5Nitisinon
19 17Nitisinone
20 1PACRITINIB CITRATE
21 1PALIFERMIN
22 2PALIVIZUMAB
23 1PEGCETACOPLAN
24 1Palifermin
25 8Pegcetacoplan
26 1Pegcetacoplanum
27 4Sodium 4-Phenylbutyrate
01 4BIOVITRUM AB
02 3Biovitrum AB (publ)
03 1SOBI
04 7SWEDISH ORPHAN
05 6SWEDISH ORPHAN BIOVITR.INT.AB
06 8SWEDISH ORPHAN BIOVITRUM AB (PUBL)
07 2SWEDISH ORPHAN BIOVITRUM AB(PU
08 4SWEDISH ORPHAN BIOVITRUM INTERNATIONAL AB
09 56Swedish Orphan Biovitrum Ab (Publ)
10 22Swedish Orphan Biovitrum Ag
11 3Swedish Orphan Biovitrum International AB
12 11Swedish Orphan Biovitrum International Ab
13 10Swedish Orphan Biovitrum Pty Ltd
14 5Swedish Orphan International AB
15 1Swedish Orphan International Ab
01 2Anakinra 100Mg 0.67 Ml 7 Joined The Parenteral Use
02 1Antic-calc Tablet
03 4CAPSULE
04 5CAPSULE;ORAL
05 4Capsule
06 4Capsule, hard
07 1Collagenase Clostridium Histolyticum 0,9Mg 1 Units Use Intralesional
08 3Film Coated Tablet
09 1Granules
10 4Hard Capsule
11 3Hard Capsule For Oral Use
12 1Hard Capsule Oral Use Hdpe
13 1INJECTABLE; INJECTION
14 2Infusion Solution
15 3Injectable Solution
16 3Injectable Solution In Pre-Filled Syringe
17 3Injection fluid, resolution
18 1Nitisinone 10Mg 60 Units Oral Use
19 1Nitisinone 2Mg 60 Units Oral Use
20 1Nitisinone 5Mg 60 Units Oral Use
21 2Oral Suspension
22 1Potion, suspension
23 20Powder And Solvent For Injectable Solution
24 1Powder For Concentrate For Infusion Solution
25 1Powder For Concentrate For Solution For Infusion
26 1Powder For Solution For Injection
27 1Powder and liquid to the injection fluid, resolution
28 2SOLUTION
29 1SUSPENSION
30 1SUSPENSION;ORAL
31 1Sodium Phenylbutyrate 266G 940Mg/G Oral Use
32 1Sodium Phenylbutyrate 500Mg 250 Unita' Oral Use
33 2Solution For Infusion
34 43Solution For Injection
35 1Solution For Perfusion
36 1TABLET
37 2VIAL
38 3VIAL; SUBCUTANEOUS
39 2injection
40 8Blank
01 10.9 mg
02 10.9mg
03 11 vial groun 0.9 mg + 1 vial solv
04 210 mg
05 2100 mg/0.67 mL
06 3100 mg/0.67 ml
07 31000IE
08 51000IU
09 11000IU/5ml
10 3100MG
11 1100MG/VIAL
12 2100mg
13 1100mg/0.67ml
14 11080MG
15 11080MG/20ML
16 11080mg
17 410MG
18 110MIU/VIAL
19 210mg
20 114400IU
21 31500IU
22 1150MG/ML
23 118MIU/VIAL
24 22 mg
25 220 mg
26 32000IE
27 52000IU
28 12000IU/5ml
29 520MG
30 320mg
31 1250 CPR 500 mg bottle
32 3250IE
33 5250IU
34 1250IU/5ml
35 125MIU/VIAL
36 32MG
37 12mg
38 73000IU
39 13000IU/5ml
40 13millionIU
41 14 000 IU
42 14 mg/ml
43 54000IU
44 14MG
45 24MG/ML
46 14mg/ml
47 25 mg
48 1500 mg
49 15000IE
50 8500IU
51 1500IU/5ml
52 150MG/VIAL
53 154mg/ml
54 35MG
55 15mg
56 16.25mg
57 160 cps 10 mg vial
58 160 cps 2 mg bottle
59 160 cps 5 mg bottle
60 16000IU
61 160MCG/KG/DAY
62 16millionIU/ml
63 27 Syringes SC 100 mg 0,67 ml
64 6750IU
65 1940 mg/g
66 1EQ 100MG BASE
67 1os granulate for suspension 266 g 940 mg/g
68 8Blank
01 10Australia
02 8Canada
03 12Italy
04 11Norway
05 31Spain
06 37Sweden
07 22Switzerland
08 12USA
Regulatory Info :
Registration Country : USA
Dosage Form : VIAL; SUBCUTANEOUS
Brand Name : KINERET
Dosage Strength : 10MIU/VIAL
Packaging :
Approval Date :
Application Number : 103950
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : VIAL; SUBCUTANEOUS
Brand Name : KINERET
Dosage Strength : 18MIU/VIAL
Packaging :
Approval Date :
Application Number : 103950
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : VIAL; SUBCUTANEOUS
Brand Name : KINERET
Dosage Strength : 25MIU/VIAL
Packaging :
Approval Date :
Application Number : 103950
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : Italy
Dosage Form : Anakinra 100Mg 0.67 Ml 7...
Brand Name : Kineret
Dosage Strength : 7 Syringes SC 100 mg 0...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Anakinra 100Mg 0.67 Ml 7...
Brand Name : Kineret
Dosage Strength : 7 Syringes SC 100 mg 0...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
Dosage Form : Injection fluid, resolut...
Brand Name : Kineret
Dosage Strength : 100 mg/0.67 ml
Packaging : Finish filled syringe
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Injection fluid, resolut...
Brand Name : Kineret
Dosage Strength : 100 mg/0.67 ml
Packaging : Finish filled syringe
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Injection fluid, resolut...
Brand Name : Kineret
Dosage Strength : 100 mg/0.67 ml
Packaging : Finish filled syringe
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Solution For Injection
Brand Name : Kineret
Dosage Strength : 100mg/0.67ml
Packaging :
Approval Date : 15/11/2013
Application Number : 20121129000048
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Injectable Solution
Brand Name : Kineret
Dosage Strength : 100mg
Packaging :
Approval Date : 08/03/2002
Application Number : 20020308000025
Regulatory Info : Deregistered
Registration Country : Sweden
