01 4ANAKINRA
02 1AVATROMBOPAG (AVATROMBOPAG MALEATE)
03 14Anakinra
04 3Avatrombopag
05 3Avatrombopag Maleate
06 3Avatrombopagmaleat
07 1Avatrombopagum
08 1Collagenase Clostridium Histolyticum
09 1Collagenase, Clostridium Histolyticum
10 21Efanesoctocog Alfa
11 7Efanesoctocog Alpha
12 7Efanesoctocog alfa
13 7Efanesoktokog alfa
14 36Efmoroctocog Alfa
15 8Efmoroctocog alfa
16 15Eftrenonacog Alfa
17 5Eftrenonacog alfa
18 5Eftrenonacogum Alfa
19 2Interferon Alpha (Leukocyte-derived)
20 2Loncastuximab Tesirine
21 1Loncastuximab tesirine
22 1Lonkastuximabtesirin
23 10NITISINONE
24 15Nitisinon
25 17Nitisinone
26 2Olezarsen
27 1PACRITINIB CITRATE
28 1PALIFERMIN
29 2PALIVIZUMAB
30 1PEGCETACOPLAN
31 1Palifermin
32 12Pegcetacoplan
33 1Pegcetacoplanum
34 2Sodium 4-Phenylbutyrate
35 8efmoroctocog alfa
36 5eftrenonacog alfa
01 4BIOVITRUM AB
02 1SOBI
03 7SWEDISH ORPHAN
04 6SWEDISH ORPHAN BIOVITR.INT.AB
05 8SWEDISH ORPHAN BIOVITRUM AB (PUBL)
06 2SWEDISH ORPHAN BIOVITRUM AB(PU
07 4SWEDISH ORPHAN BIOVITRUM INTERNATIONAL AB
08 7Swedish Orphan Biovitrum AB
09 3Swedish Orphan Biovitrum AB (1)
10 26Swedish Orphan Biovitrum Ab
11 81Swedish Orphan Biovitrum Ab (Publ)
12 22Swedish Orphan Biovitrum Ag
13 5Swedish Orphan Biovitrum Interna
14 18Swedish Orphan Biovitrum International AB
15 16Swedish Orphan Biovitrum International Ab
16 12Swedish Orphan Biovitrum Pty Ltd
17 3Swedish Orphan International AB
18 1Swedish Orphan International Ab
01 2Anakinra 100Mg 0.67 Ml 7 Joined The Parenteral Use
02 4CAPSULE
03 5CAPSULE;ORAL
04 12Capsule
05 1Collagenase Clostridium Histolyticum 0,9Mg 1 Units Use Intralesional
06 7Film Coated Tablet
07 1Film-Coated Tablet
08 4Hard Capsule
09 3Hard Capsule For Oral Use
10 1Hard Capsule Oral Use Hdpe
11 4Hard Capsules
12 1INJECTABLE; INJECTION
13 3Infusion Solution
14 3Injectable Solution
15 1Injectable Solution In Pre-Filled Pen
16 3Injectable Solution In Pre-Filled Syringe
17 1Nitisinone 10Mg 60 Units Oral Use
18 1Nitisinone 2Mg 60 Units Oral Use
19 1Nitisinone 5Mg 60 Units Oral Use
20 5Oral Suspension
21 20Powder And Solvent For Injectable Solution
22 22Powder And Solvents For Solution For Injection
23 1Powder For Concentrate For Infusion Solution
24 3Powder For Concentrate For Solution For Infusion
25 1Powder For Solution For Injection
26 2SOLUTION
27 1SUSPENSION
28 1SUSPENSION;ORAL
29 1Sodium Phenylbutyrate 266G 940Mg/G Oral Use
30 1Sodium Phenylbutyrate 500Mg 250 Unita' Oral Use
31 3Solution For Infusion
32 88Solution For Injection
33 1Solution For Perfusion
34 1TABLET
35 2VIAL
36 3VIAL; SUBCUTANEOUS
37 2injection
38 10Blank
01 10.9mg
02 11 vial groun 0.9 mg + 1 vial solv
03 110 mg
04 2100 mg/0.67 mL
05 31000 IU
06 31000IE
07 111000IU
08 11000IU/5ml
09 3100MG
10 1100MG/VIAL
11 2100mg
12 4100mg/0.67ml
13 11080MG
14 11080MG/20ML
15 21080mg
16 11080mg/20ml
17 410MG
18 110MIU/VIAL
19 710mg
20 114400IU
21 11500 IU
22 51500IU
23 1150MG/ML
24 1150mg/ml
25 118MIU/VIAL
26 12 mg
27 120 mg
28 32000 IU
29 32000IE
30 112000IU
31 12000IU/5ml
32 520MG
33 1120mg
34 1250 CPR 500 mg bottle
35 3250 IU
36 3250IE
37 11250IU
38 1250IU/5ml
39 125MIU/VIAL
40 32MG
41 32mg
42 33000 IU
43 133000IU
44 13000IU/5ml
45 13millionIU
46 14 000 IU
47 14000 IE
48 14000 IU
49 14000IE
50 84000IU
51 14MG
52 24MG/ML
53 34mg/ml
54 15 mg
55 3500 IU
56 15000 IU
57 15000IE
58 14500IU
59 1500IU/5ml
60 150MG/VIAL
61 154mg/ml
62 35MG
63 35mg
64 16.25mg
65 160 cps 10 mg vial
66 160 cps 2 mg bottle
67 160 cps 5 mg bottle
68 16000 IU
69 16000IU
70 160MCG/KG/DAY
71 16millionIU/ml
72 27 Syringes SC 100 mg 0,67 ml
73 1750 IE
74 1750 IU
75 1750IE
76 9750IU
77 180MG
78 180mg
79 1EQ 100MG BASE
80 1os granulate for suspension 266 g 940 mg/g
81 13Blank
01 12Australia
02 8Canada
03 31Denmark
04 29Estonia
05 12Italy
06 30Norway
07 32Spain
08 38Sweden
09 22Switzerland
10 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 : Marketed
Registration Country : Norway
Dosage Form : Solution For Injection
Brand Name : Kineret
Dosage Strength : 100mg/0.67ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Solution For Injection
Brand Name : Kineret
Dosage Strength : 100mg/0.67ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
Regulatory Info : Prescription
Registration Country : Estonia
Dosage Form : Solution For Injection
Brand Name : Kineret
Dosage Strength : 150mg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia
Regulatory Info : Cancelled
Registration Country : Spain
Dosage Form : Injectable Solution In P...
Brand Name : Kineret
Dosage Strength : 100MG
Packaging :
Approval Date : 10-04-2002
Application Number : 2203003
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Cancelled
Registration Country : Spain
Dosage Form : Injectable Solution In P...
Brand Name : Kineret
Dosage Strength : 100MG
Packaging :
Approval Date : 10-04-2002
Application Number : 2203002
Regulatory Info : Cancelled
Registration Country : Spain
