01 2ALBUMIN (HUMAN)
02 3ANTIHEMOPHILIC FACTOR (HUMAN)
03 4C1 ESTERASE INHIBITOR (HUMAN)
04 2COAGULATION FACTOR II (HUMAN)
05 2COAGULATION FACTOR IX (HUMAN)
06 2COAGULATION FACTOR VII (HUMAN)
07 2COAGULATION FACTOR X (HUMAN)
08 2FACTOR XIII
09 1FIBRINOGEN (HUMAN)
10 6IMMUNOGLOBULIN (HUMAN)
11 2PROTEIN C
12 2PROTEIN S
13 3VON WILLEBRAND FACTOR (HUMAN)
01 4KIT
02 21POWDER FOR SOLUTION
03 8SOLUTION
01 110%
02 11000MG/VIAL
03 11000UNIT
04 11020UNIT
05 11200UNIT/15ML
06 11240UNIT
07 11250UNIT/VIAL
08 11360UNIT
09 11500UNIT/VIAL
10 11600UNIT
11 11640UNIT
12 11680UNIT/10ML
13 12000UNIT/VIAL
14 5200MG/ML
15 12040UNIT
16 125%
17 1250UNIT/VIAL
18 13000UNIT/VIAL
19 1300UNIT/5ML
20 13360UNIT/15ML
21 15%
22 1500UNIT
23 1500UNIT/VIAL
24 1600UNIT/10ML
25 1620UNIT
26 1680UNIT
27 1800UNIT
28 1820UNIT
29 1840UNIT/5ML
01 1ALBUREX - 25
02 1ALBUREX - 5
03 1BERINERT 1500
04 1BERINERT 500
05 6BERIPLEX P/N 1000
06 6BERIPLEX P/N 500
07 1CORIFACT 1250
08 1CORIFACT 250
09 2HAEGARDA
10 5HIZENTRA
11 6HUMATE-P
12 1PRIVIGEN
13 1RIASTAP
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : SOLUTION
Dosage Strength : 5%
Packaging : 100ML/250ML/500ML
Brand Name : ALBUREX - 5
Approval Date :
Application Number : 2274655
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : SOLUTION
Dosage Strength : 25%
Packaging : 50ML/100ML
Brand Name : ALBUREX - 25
Approval Date :
Application Number : 2274663
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 1200UNIT/15ML
Packaging : 15ML
Brand Name : HUMATE-P
Approval Date :
Application Number : 2261235
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 300UNIT/5ML
Packaging : 5ML
Brand Name : HUMATE-P
Approval Date :
Application Number : 2261219
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 600UNIT/10ML
Packaging : 10ML
Brand Name : HUMATE-P
Approval Date :
Application Number : 2261227
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : KIT
Dosage Strength : 1500UNIT/VIAL
Packaging : 3ML
Brand Name : BERINERT 1500
Approval Date :
Application Number : 2436078
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : KIT
Dosage Strength : 2000UNIT/VIAL
Packaging : 4ML
Brand Name : HAEGARDA
Approval Date :
Application Number : 2468069
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : KIT
Dosage Strength : 3000UNIT/VIAL
Packaging :
Brand Name : HAEGARDA
Approval Date :
Application Number : 2468077
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : KIT
Dosage Strength : 500UNIT/VIAL
Packaging : 10ML
Brand Name : BERINERT 500
Approval Date :
Application Number : 2352575
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 1600UNIT
Packaging : 50ML
Brand Name : BERIPLEX P/N 1000
Approval Date :
Application Number : 2410826
Regulatory Info : Schedule D
Registration Country : Canada
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