01 1ALBUMIN (HUMAN)
02 2ANTIHEMOPHILIC FACTOR (HUMAN)
03 2Albumin, Human
04 8Albumin, Humant
05 1Anti-D Immunoglobulin 125 µg
06 1Anti-D Immunoglobulin 250 µg
07 5Anti-D Immunoglobulin, Human
08 1Antithrombin III Human
09 2COAGULATION FACTOR II (HUMAN)
10 2COAGULATION FACTOR IX (HUMAN)
11 2COAGULATION FACTOR VII (HUMAN)
12 2COAGULATION FACTOR X (HUMAN)
13 1Calcium
14 2Coagulation Factor II (Prothrombin, Human); Factor IX (Human); Factor VII (Human); Factor X (Human); Protein C (Human); Protein S (Human)
15 5Coagulation Factor Ix, Human
16 4Coagulation Factor VIII Human; Von Willebrand Factor Human
17 1Ecallantide
18 1FIBRINOGEN (HUMAN)
19 2Factor Ix
20 5Factor Viii, Human
21 2Fibrinogen, Human
22 3HUMAN PLASMA PROTEINS
23 6Human Albumin
24 2Human Albumin Solution
25 1Human Anti-Hepatitis B Immunoglobulin
26 2Human Antithrombin Iii
27 3Human Coagulation Factor IX
28 2Human Coagulation Factor Ix
29 3Human Coagulation Factor VIII
30 1Human Coagulation II,VII,IX,X
31 1Human Coagulation IX
32 1Human Coagulation VII
33 1Human Coagulation X
34 4Human Factor Viii
35 2Human Fibrinogen
36 10Human Normal Immunoglobulin
37 1Human Normal Immunoglobulin (Igg)
38 3Human Normal Immunoglobulin G
39 14Human Plasma Protein
40 2Human Von Willebrand Factor; Human Coagulation Factor Viii
41 30Immunoglobulin G 285-292
42 2Immunoglobulin G, Human
43 9Immunoglobulin, Human Normal
44 5Koagulationsfaktor Viii, Human
45 7Normal Human Immunoglobulin
46 2PROTEIN C
47 2PROTEIN S
48 5Perflutren
49 2Plasma Proteins (Human)
50 8Plasma protein fraction, human
51 1Protein C
52 1Protein S
53 23Simoctocog Alfa
54 4Simoctocogum Alfa
55 1Total Protein
56 2VON WILLEBRAND FACTOR (HUMAN)
01 13OCTAPHARMA ITALY SPA
02 6OCTAPHARMA LTD
03 1OCTAPHARMA PHARMAZEUTIKA GMBH
04 21OCTAPHARMA PHARMAZEUTIKA PRODUKTIONSGES M B H
05 13Octapharma (2)
06 26Octapharma (IP) SPRL
07 8Octapharma AB
08 4Octapharma AS
09 66Octapharma Ab
10 4Octapharma Ag
11 24Octapharma SA (Pty) Ltd
12 32Octapharma Sa
01 18.2
02 1Coagulation Factor Ix Lyophilized Human 1.000Iu 10Ml 1 Units Parenteral Use
03 1Human Albumin 20% 100Ml 1 Units Parenteral Use
04 1Human Albumin 20% 50Ml 1 Units Parenteral Use
05 1Human Albumin 25% 50Ml 1 Units Parenteral Use
06 1Human Immunoglobulin Anti-D 625Iu 1Ml 1 Units Parenteral Use
07 1Human Immunoglobulin Anti-D 625Iu 2Ml 1 Units Parenteral Use
08 1Human Normal Immunoglobulin 1.65G 10Ml 1 Units Parenteral Use
09 1Human Normal Immunoglobulin 1.65G 10Ml 10 Units Parenteral Use
10 1Human Normal Immunoglobulin 1.65G 10Ml 20 Joined The Parenteral Use
11 1Human Normal Immunoglobulin 10G 100Ml 1 Units Parenteral Use
12 1Human Normal Immunoglobulin 10G 200Ml 1 Units Parenteral Use
13 1Human Normal Immunoglobulin 2,5G 50Ml 1 Units Parenteral Use
14 1Human Normal Immunoglobulin 20G 200Ml 1 Units Parenteral Use
15 1Human Normal Immunoglobulin 2G 20Ml 1 Units Parenteral Use
16 1Human Normal Immunoglobulin 3. 3G 20Ml 1 Units Parenteral Use
17 1Human Normal Immunoglobulin 3. 3G 20Ml 10 Units Parenteral Use
18 1Human Normal Immunoglobulin 3. 3G 20Ml 20 Joined The Parenteral Use
19 1Human Normal Immunoglobulin 5G 100Ml 1 Units Parenteral Use
20 1Human Normal Immunoglobulin 5G 50Ml 1 Units Parenteral Use
21 1Human Plasma Proteins 200Ml 1 Units Parenteral Use
22 3INF
23 19INJ
24 13Infusion Solution
25 9Infusion fluid, resolution
26 6Injectable Solution
27 8Injection fluid, resolution
28 2Injection/Infusion Solution
29 12KIT
30 7POWDER FOR SOLUTION
31 6Powder And Solvent For Infusion Solution
32 14Powder And Solvent For Injectable Solution
33 1Powder And Solvent For Injectable Solution And Infusion
34 1Powder And Solvent For Injection And Infusion Solution
35 9Powder And Solvent For Injection Solution
36 4Powder and liquid for infusion, solution
37 1SOL
38 2SOLUTION
39 1Solution
40 16Solution For Infusion
41 40Solution For Injection
42 18Solution For Perfusion
43 4Solution for infusion
44 1Subcutaneous Injectable Solution
01 11 bag EV 200 ml
02 11 bottle EV 100 ml 100 mg/ml
03 11 bottle EV 100 ml 20% 200 g/l
04 11 bottle EV 100 ml 5%
05 11 bottle EV 20 ml 100 mg/ml
06 11 bottle EV 200 ml 100 mg/ml
07 11 bottle EV 200 ml 5%
08 11 bottle EV 50 ml 100 mg/ml
09 11 bottle EV 50 ml 20% 200 g/l
10 11 bottle EV 50 ml 25% 250 g/l
11 11 bottle EV 50 ml 5%
12 11 vial IM 1 ml 625 IU/ml
13 11 vial IM 2 ml 625 IU/ml
14 11 vial SC 10 ml 165 mg/ml
15 11 vial SC 20 ml 165 mg/ml
16 11 vial groun 1000 IU + 1 vial solv 10 ml
17 110 VIALS SC 10 ml 165 mg/ml
18 110 VIALS SC 20 ml 165 mg/ml
19 4100 mg/ml
20 51000IE
21 11000IEVWF/1000IEFVIII
22 31000IU
23 21000IU/10 ml
24 11000IU/5ml
25 11000IU; 1000IU
26 21000UNIT/10ML
27 11000UNIT/VIAL
28 4100IU
29 2100IU/ML
30 2100IU/ml
31 4100MG
32 2100MG/ML
33 1100MGI/ML
34 1100MMOL/ML
35 2100mg/ml
36 1100ml
37 11200UNIT/VIAL
38 11240UNIT/VIAL
39 11250IE
40 11250IU
41 11280UNIT/VIAL
42 114G/200ML
43 21500IU
44 11520UNIT/VIAL
45 115MG/10ML
46 8165 mg/ml
47 2165MG
48 2165MG/ML
49 7165mg/ml
50 11G
51 11G/VIAL
52 21g
53 120 VIALS SC 10 ml 165 mg/ml
54 120 VIALS SC 20 ml 165 mg/ml
55 1200 g/l
56 22000IE
57 12000IU
58 12000IU/5ml
59 2200G
60 2200G/L
61 2200IE/ml
62 2200IU
63 1200IU/ML
64 2200g/1000 ml
65 3200g/l
66 120MG/ML
67 125%
68 22500IE
69 12500IU
70 2250IE
71 1250IU
72 2250IU/5 ml
73 1250IU/5ml
74 1250g/l
75 33000IU
76 34000IU
77 240g/l
78 845-70 mg/ml
79 145-70MG/ML
80 1450IEFVIII/400IEVWF
81 1480UNIT/VIAL
82 150 g/l
83 350 mg/ml
84 1500IEVWF/500IEFVIII
85 8500IU
86 1500IU/10 ml
87 8500IU/5 ml
88 1500IU/5ml
89 1500IU; 500IU
90 2500UNIT/5ML
91 1500UNIT/VIAL
92 250G
93 250G/L
94 150IU
95 150IU/ML
96 250IU/ml
97 250MG
98 150MG/ML
99 250g/l
100 550mg/ml
101 1600UNIT/VIAL
102 1620UNIT/VIAL
103 2625IE/ml
104 1625IU
105 1625IU/ML
106 1640UNIT/VIAL
107 17.5MG/5ML
108 1270MG
109 1750IU/ml
110 1760UNIT/VIAL
111 19-14G
112 1900IEFVIII/800IEVWF
113 1960UNIT/VIAL
114 6Blank
01 21Canada
02 20Italy
03 26Malta
04 25Norway
05 24South Africa
06 40Spain
07 58Sweden
08 4Switzerland
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : OCTALBIN 25%
Dosage Strength : 25%
Packaging : 50ML/100ML
Approval Date :
Application Number : 2267357
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Solution For Infusion
Brand Name : Albunorm
Dosage Strength : 50G/L
Packaging :
Approval Date : 2010-05-17
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Solution For Infusion
Brand Name : Albunorm
Dosage Strength : 200G/L
Packaging :
Approval Date : 2010-05-17
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Infusion Solution
Brand Name : Albumin Octapharma
Dosage Strength : 200g/l
Packaging :
Approval Date : 04/11/1999
Application Number : 19991104000028
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Infusion Solution
Brand Name : Albumin Octapharma
Dosage Strength : 50g/l
Packaging :
Approval Date : 04/11/1999
Application Number : 19991104000011
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Infusion Solution
Brand Name : Albunorm
Dosage Strength : 200g/l
Packaging :
Approval Date : 29/05/2009
Application Number : 20080516000026
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Infusion Solution
Brand Name : Albunorm
Dosage Strength : 250g/l
Packaging :
Approval Date : 18/06/2010
Application Number : 20091115000027
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Infusion Solution
Brand Name : Albunorm
Dosage Strength : 40g/l
Packaging :
Approval Date : 18/06/2010
Application Number : 20091115000010
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Infusion Solution
Brand Name : Albunorm
Dosage Strength : 50g/l
Packaging :
Approval Date : 29/05/2009
Application Number : 20080516000019
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Infusion Solution
Brand Name : Albuminativ
Dosage Strength : 200g/l
Packaging :
Approval Date : 29/03/1955
Application Number : 19550329000017
Regulatory Info : Deregistered
Registration Country : Sweden
