01 10Anakinra
02 2Avatrombopag Maleate
03 3Avatrombopagmaleat
04 1Avatrombopagum
05 1Collagenase Clostridium Histolyticum
06 1Collagenase, Clostridium Histolyticum
07 14Efanesoctocog Alfa
08 7Efanesoctocog Alpha
09 7Efanesoktokog alfa
10 26Efmoroctocog Alfa
11 8Efmoroctocog alfa
12 10Eftrenonacog Alfa
13 5Eftrenonacog alfa
14 5Eftrenonacogum Alfa
15 2Interferon Alpha (Leukocyte-derived)
16 1Loncastuximab Tesirine
17 1Lonkastuximabtesirin
18 10Nitisinon
19 12Nitisinone
20 1Palifermin
21 2Pegcetacoplan
22 1Pegcetacoplanum
23 2Sodium 4-Phenylbutyrate
01 2Anakinra 100Mg 0.67 Ml 7 Joined The Parenteral Use
02 8Capsule
03 1Collagenase Clostridium Histolyticum 0,9Mg 1 Units Use Intralesional
04 6Film Coated Tablet
05 4Hard Capsule
06 3Hard Capsule For Oral Use
07 1Hard Capsule Oral Use Hdpe
08 2Infusion Solution
09 3Injectable Solution
10 3Injectable Solution In Pre-Filled Syringe
11 1Nitisinone 10Mg 60 Units Oral Use
12 1Nitisinone 2Mg 60 Units Oral Use
13 1Nitisinone 5Mg 60 Units Oral Use
14 3Oral Suspension
15 20Powder And Solvent For Injectable Solution
16 1Powder For Concentrate For Infusion Solution
17 1Powder For Concentrate For Solution For Infusion
18 1Powder For Solution For Injection
19 1Sodium Phenylbutyrate 266G 940Mg/G Oral Use
20 1Sodium Phenylbutyrate 500Mg 250 Unita' Oral Use
21 2Solution For Infusion
22 65Solution For Injection
23 1Solution For Perfusion
01 10.9mg
02 11 vial groun 0.9 mg + 1 vial solv
03 110 mg
04 31000IE
05 81000IU
06 11000IU/5ml
07 3100MG
08 2100mg
09 3100mg/0.67ml
10 11080MG
11 11080mg
12 210MG
13 310mg
14 114400IU
15 41500IU
16 12 mg
17 120 mg
18 32000IE
19 82000IU
20 12000IU/5ml
21 220MG
22 720mg
23 1250 CPR 500 mg bottle
24 3250IE
25 8250IU
26 1250IU/5ml
27 12MG
28 22mg
29 103000IU
30 13000IU/5ml
31 13millionIU
32 14 000 IU
33 14000IE
34 64000IU
35 14MG
36 24mg/ml
37 15 mg
38 15000IE
39 11500IU
40 1500IU/5ml
41 154mg/ml
42 15MG
43 15mg
44 16.25mg
45 160 cps 10 mg vial
46 160 cps 2 mg bottle
47 160 cps 5 mg bottle
48 16000IU
49 16millionIU/ml
50 27 Syringes SC 100 mg 0,67 ml
51 1750IE
52 7750IU
53 1os granulate for suspension 266 g 940 mg/g
54 1Blank
01 12Italy
02 30Norway
03 31Spain
04 37Sweden
05 22Switzerland
01 18Alprolix
02 2Alprolix IE
03 25Altuvoct
04 3Altuvoct IE
05 2Ammonaps
06 3Aspaveli
07 1Baptism
08 5Doptelet
09 29Elocta
10 5Elocta IE
11 1Kepivance
12 10Kineret
13 2Multiferon
14 4ORFADIN
15 18Orfadin
16 2Xiapex
17 2Zynlonta
Regulatory Info :
Registration Country : Italy
Dosage Form : Anakinra 100Mg 0.67 Ml 7 Joine...
Dosage Strength : 7 Syringes SC 100 mg 0,67 m...
Packaging :
Brand Name : Kineret
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Anakinra 100Mg 0.67 Ml 7 Joine...
Dosage Strength : 7 Syringes SC 100 mg 0,67 m...
Packaging :
Brand Name : Kineret
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Solution For Injection
Dosage Strength : 100mg/0.67ml
Packaging :
Brand Name : Kineret
Approval Date : 15/11/2013
Application Number : 20121129000048
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Injectable Solution
Dosage Strength : 100mg
Packaging :
Brand Name : Kineret
Approval Date : 08/03/2002
Application Number : 20020308000025
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Solution For Injection
Dosage Strength : 100mg
Packaging :
Brand Name : Kineret
Approval Date : 08/03/2002
Application Number : 20020308000018
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Cancelled
Registration Country : Spain
Dosage Form : Injectable Solution In Pre-Fil...
Dosage Strength : 100MG
Packaging :
Brand Name : Kineret
Approval Date : 2002-04-10
Application Number : 02203003
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Cancelled
Registration Country : Spain
Dosage Form : Injectable Solution In Pre-Fil...
Dosage Strength : 100MG
Packaging :
Brand Name : Kineret
Approval Date : 2002-04-10
Application Number : 02203002
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Injectable Solution In Pre-Fil...
Dosage Strength : 100MG
Packaging :
Brand Name : Kineret
Approval Date : 2015-01-15
Application Number : 102203006
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Solution For Injection
Dosage Strength : 100mg/0.67ml
Packaging :
Brand Name : Kineret
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Solution For Injection
Dosage Strength : 100mg/0.67ml
Packaging :
Brand Name : Kineret
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
