01 2ALBUMIN (HUMAN)
02 3ANTIHEMOPHILIC FACTOR (HUMAN)
03 4Albuminum humanum
04 5Albutrepenonacogum alfa
05 2Alpha-1-proteinasi inhibitor humanum
06 4C1 ESTERASE INHIBITOR (HUMAN)
07 2COAGULATION FACTOR II (HUMAN)
08 2COAGULATION FACTOR IX (HUMAN)
09 2COAGULATION FACTOR VII (HUMAN)
10 2COAGULATION FACTOR X (HUMAN)
11 2Calcium
12 2FACTOR XIII
13 1FIBRINOGEN (HUMAN)
14 4Factor VIII coagulationis humanus; Factor humanus von Willebrandi
15 2Factor XIII coagulation humanus
16 4Flera substanser, se innehåll
17 1Human C1-esterase inhibitor
18 2Human Coagulation Factor II (Prothrombin); Human Coagulation Factor VII; Human Coagulation Factor IX; Human Coagulation Factor X; Human Protein C; Human Protein S
19 2Human coagulation factor VIII
20 2Human fibrinogen
21 6IMMUNOGLOBULIN (HUMAN)
22 1Immunglobulin anti-D, human
23 8Immunoglobulin G 285-292
24 1Immunoglobulinum humanum anti-D
25 9Immunoglobulinum humanum normal
26 3Lonoctocogum alfa
27 2PROTEIN C
28 2PROTEIN S
29 4Perflutren
30 5Several substances refer to content
31 2Tetanus vaccine
32 3VON WILLEBRAND FACTOR (HUMAN)
33 4albumin, human
34 1alfa-1-proteinashämmare
35 2anti-D immunglobulin, humant
36 2coagulation factor XIII, human
37 2complement factor 1 (C1) -esterashämmare
38 1fibrinogen, humant
39 1immunglobulin, humant normalt
40 2immunoglobulins, normal human
41 1immunoglobulins, normal human, for
42 1koagulationsfaktor IX, human
01 33CSL BEHRING CANADA INC
02 15CSL BEHRING GmbH
03 1CSL BEHRING SpA
04 29CSL Behring AG
05 27CSL Behring GmbH
06 8CSL Behring Lengnau AG
01 1Coagulation Factor Ix Lyophilized Human 1.000Iu 10Ml 1 Units Parenteral Use
02 1Coagulation Factor Ix Lyophilized Human 500Iu 5Ml 1 Units Parenteral Use
03 11Dry Sub
04 2Dry Sub Cum Solv
05 1Human Albumin 20% 100Ml 1 Units Parenteral Use
06 2Human Albumin 20% 50Ml 1 Units Parenteral Use
07 1Human Albumin 25% 50Ml 1 Units Parenteral Use
08 1Human Immunoglobulin Anti-Tetanus 250Iu 1Ml 1 Units Parenteral Use
09 1Human Immunoglobulin Anti-Tetanus 500Iu 2Ml 1 Units Parenteral Use
10 1Human Normal Immunoglobulin 10G 100Ml 1 Units Parenteral Use
11 1Human Normal Immunoglobulin 10G 50Ml 1 Units Parenteral Use
12 1Human Normal Immunoglobulin 1G 5Ml 1 Units Parenteral Use
13 1Human Normal Immunoglobulin 2,5G 25Ml 1 Units Parenteral Use
14 1Human Normal Immunoglobulin 20G 200Ml 1 Units Parenteral Use
15 1Human Normal Immunoglobulin 2G 10Ml 1 Units Parenteral Use
16 1Human Normal Immunoglobulin 4G 20Ml 1 Units Parenteral Use
17 1Human Normal Immunoglobulin 5G 50Ml 1 Units Parenteral Use
18 1INJEKTIONSVÄTSKA, LÖSNING
19 2INJEKTIONSVÄTSKA, LÖSNING, FÖRFYLLD SPRUTA
20 2Inf L?s
21 4Inf Loose
22 1Inf Soluble
23 2Inf Solution
24 1Inj Solution
25 4Inj. L?s
26 4KIT
27 9POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
28 21POWDER FOR SOLUTION
29 1PULVER OCH VÄTSKA TILL INFUSIONSVÄTSKA
30 5PULVER OCH VÄTSKA TILL INJEKTIONS-
31 1PULVER TILL INJEKTIONS-/INFUSIONSVÄTSKA
32 8SOLUTION
33 5SOLUTION FOR INFUSION
34 1SOLUTION FOR INJECTION
35 1SOLUTION FOR INJECTION, PRE-FILLED SYRINGE
36 1Solution for injection, solution in pre-filled syringe
37 8Trockensub
38 2Trockensub Mit Solv
01 11 G
02 11 ampoule EV 1,000 IU + 1 ampoule solv 10 ml + Kit
03 11 ampoule EV 500 IU + 1 ampoule solv 5 ml + Kit
04 11 bottle EV 100 ml 100 mg/ml
05 11 bottle EV 100 ml 20%
06 11 bottle EV 200 ml 100 mg/ml
07 11 bottle EV 25 ml 100 mg/ml
08 11 bottle EV 50 ml 100 mg/ml
09 11 bottle EV 50 ml 200 g/l
10 11 bottle EV 50 ml 25%
11 11 syringe EV 500 IU 2 ml
12 11 syringe IM 250 IU 1 ml
13 11 vial EV 50 ml 20%
14 11 vial SC 10 ml 200 mg/ml
15 11 vial SC 20 ml 200 mg/ml
16 11 vial SC 5 ml 200 mg/ml
17 11 vial SC 50 ml 200 mg/ml
18 110%
19 1100 IE/ML
20 1100 MG / ML
21 11000 IE (200
22 11000 IE FVIII
23 11000 IU
24 11000 IU FVIII /
25 11000 MG
26 11000/2400Ie
27 11000IE
28 11000MG/VIAL
29 11000UNIT
30 21000iu
31 11000iu/2400ml
32 11000mg
33 11020UNIT
34 110g/100ml
35 110g/50ml
36 11200UNIT/15ML
37 11240UNIT
38 11250 IU
39 11250UNIT/VIAL
40 11250iu
41 11360UNIT
42 11500 IE (300
43 11500 IU
44 11500 IU/2 ml
45 11500UNIT/VIAL
46 1160 MG / ML
47 1160 MG/ML
48 11600UNIT
49 11640UNIT
50 11680UNIT/10ML
51 11g
52 11g/5ml
53 12.5g/25ml
54 220%
55 2200 G / L
56 1200 MG / ML
57 12000IE
58 12000UNIT/VIAL
59 12000iu
60 5200MG/ML
61 12040UNIT
62 120g/200ml
63 125%
64 1250 IE FVIII
65 2250 IU
66 1250UNIT/VIAL
67 2250iu
68 12g
69 12g/10ml
70 13000UNIT/VIAL
71 1300UNIT/5ML
72 1300mcg/2ml
73 13360UNIT/15ML
74 13500iu
75 14000mg
76 140g/400ml
77 14g/20ml
78 35%
79 250 G / L
80 2500 IE FVIII
81 2500 IU
82 1500 IU FVIII /
83 1500/1200Ie
84 3500IE
85 1500UNIT
86 1500UNIT/VIAL
87 1500iu
88 1500iu/1200
89 15g/50ml
90 1600UNIT/10ML
91 1620UNIT
92 1680UNIT
93 1800UNIT
94 1820UNIT
95 1840UNIT/5ML
96 2Blank
01 33Canada
02 16Italy
03 1Norway
04 26Sweden
05 37Switzerland
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : ALBUREX - 5
Dosage Strength : 5%
Packaging : 100ML/250ML/500ML
Approval Date :
Application Number : 2274655
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : ALBUREX - 25
Dosage Strength : 25%
Packaging : 50ML/100ML
Approval Date :
Application Number : 2274663
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info :
Registration Country : Sweden
Dosage Form : SOLUTION FOR INFUSION
Brand Name : Albumin Behring
Dosage Strength : 200 G / L
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Dosage Form : SOLUTION FOR INFUSION
Brand Name : Albumin Behring
Dosage Strength : 50 G / L
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Dosage Form : SOLUTION FOR INFUSION
Brand Name : Alburex
Dosage Strength : 50 G / L
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Dosage Form : SOLUTION FOR INFUSION
Brand Name : Alburex
Dosage Strength : 200 G / L
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Switzerland
Dosage Form : Inf Loose
Brand Name : Albumin CSL 20%
Dosage Strength : 20%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Dosage Form : Inf Loose
Brand Name : Albumin CSL 20%
Dosage Strength : 20%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Dosage Form : Inf Loose
Brand Name : Albumin CSL 5%
Dosage Strength : 5%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Dosage Form : Inf Loose
Brand Name : Albumin CSL 5%
Dosage Strength : 5%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
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