01 4ANAKINRA
02 1AVATROMBOPAG (AVATROMBOPAG MALEATE)
03 10Anakinra
04 2Avatrombopag
05 1Avatrombopag Maleate
06 1Avatrombopagum
07 2Collagenase Clostridium Histolyticum
08 1Collagenase, Clostridium Histolyticum
09 14Efanesoctocog Alfa
10 18Efmoroctocog Alfa
11 5Eftrenonacog Alfa
12 5Eftrenonacogum Alfa
13 2Interferon Alpha (Leukocyte-derived)
14 1Lonkastuximabtesirin
15 10NITISINONE
16 5Nitisinon
17 12Nitisinone
18 1PACRITINIB CITRATE
19 1PALIFERMIN
20 2PALIVIZUMAB
21 1PEGCETACOPLAN
22 1Palifermin
23 7Pegcetacoplan
24 1Pegcetacoplanum
25 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 30Swedish Orphan Biovitrum Ab (Publ)
10 22Swedish Orphan Biovitrum Ag
11 3Swedish Orphan Biovitrum International AB
12 6Swedish 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 2Film Coated Tablet
09 1Granules
10 3Hard Capsule For Oral Use
11 1Hard Capsule Oral Use Hdpe
12 1INJECTABLE; INJECTION
13 2Infusion Solution
14 3Injectable Solution
15 3Injection fluid, resolution
16 1Nitisinone 10Mg 60 Units Oral Use
17 1Nitisinone 2Mg 60 Units Oral Use
18 1Nitisinone 5Mg 60 Units Oral Use
19 1Oral Suspension
20 1Potion, suspension
21 1Powder For Concentrate For Solution For Infusion
22 1Powder For Solution For Injection
23 1Powder and liquid to the injection fluid, resolution
24 2SOLUTION
25 1SUSPENSION
26 1SUSPENSION;ORAL
27 1Sodium Phenylbutyrate 266G 940Mg/G Oral Use
28 1Sodium Phenylbutyrate 500Mg 250 Unita' Oral Use
29 2Solution For Infusion
30 43Solution For Injection
31 1TABLET
32 2VIAL
33 3VIAL; SUBCUTANEOUS
34 2injection
35 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 21000IU
09 11000IU/5ml
10 1100MG/VIAL
11 2100mg
12 1100mg/0.67ml
13 11080MG/20ML
14 11080mg
15 210MG
16 110MIU/VIAL
17 210mg
18 21500IU
19 1150MG/ML
20 118MIU/VIAL
21 22 mg
22 220 mg
23 32000IE
24 22000IU
25 12000IU/5ml
26 320MG
27 320mg
28 1250 CPR 500 mg bottle
29 3250IE
30 2250IU
31 1250IU/5ml
32 125MIU/VIAL
33 22MG
34 12mg
35 53000IU
36 13000IU/5ml
37 13millionIU
38 14 mg/ml
39 44000IU
40 24MG/ML
41 14mg/ml
42 25 mg
43 1500 mg
44 15000IE
45 5500IU
46 1500IU/5ml
47 150MG/VIAL
48 154mg/ml
49 25MG
50 15mg
51 16.25mg
52 160 cps 10 mg vial
53 160 cps 2 mg bottle
54 160 cps 5 mg bottle
55 16000IU
56 160MCG/KG/DAY
57 16millionIU/ml
58 27 Syringes SC 100 mg 0,67 ml
59 4750IU
60 1940 mg/g
61 1EQ 100MG BASE
62 1os granulate for suspension 266 g 940 mg/g
63 8Blank
01 10Australia
02 8Canada
03 12Italy
04 11Norway
05 37Sweden
06 22Switzerland
07 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 : 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 : Canada
Dosage Form : SOLUTION
Brand Name : KINERET
Dosage Strength : 150MG/ML
Packaging : 0.67 ML
Approval Date :
Application Number : 2245913
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Australia
Dosage Form : injection
Brand Name : Kineret
Dosage Strength : 100 mg/0.67 mL
Packaging : 28
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
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
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Solution For Injection
Brand Name : Kineret
Dosage Strength : 100mg
Packaging :
Approval Date : 08/03/2002
Application Number : 20020308000018
Regulatory Info : Deregistered
Registration Country : Sweden
