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01 1ALBUMIN (HUMAN)
02 2ANTIHEMOPHILIC FACTOR (HUMAN)
03 2COAGULATION FACTOR II (HUMAN)
04 2COAGULATION FACTOR IX (HUMAN)
05 2COAGULATION FACTOR VII (HUMAN)
06 2COAGULATION FACTOR X (HUMAN)
07 1FIBRINOGEN (HUMAN)
08 3HUMAN PLASMA PROTEINS
09 2PROTEIN C
10 2PROTEIN S
11 2VON WILLEBRAND FACTOR (HUMAN)
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01 6KIT
02 13POWDER FOR SOLUTION
03 2SOLUTION
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01 21000UNIT/10ML
02 11000UNIT/VIAL
03 11200UNIT/VIAL
04 11240UNIT/VIAL
05 11280UNIT/VIAL
06 114G/200ML
07 11520UNIT/VIAL
08 115MG/10ML
09 11G/VIAL
10 125%
11 1480UNIT/VIAL
12 2500UNIT/5ML
13 1500UNIT/VIAL
14 1600UNIT/VIAL
15 1620UNIT/VIAL
16 1640UNIT/VIAL
17 17.5MG/5ML
18 1760UNIT/VIAL
19 1960UNIT/VIAL
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01 1FIBRYGA
02 1OCTALBIN 25%
03 1OCTAPLASMA
04 12OCTAPLEX
05 6WILATE
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : SOLUTION
Dosage Strength : 25%
Packaging : 50ML/100ML
Brand Name : OCTALBIN 25%
Approval Date :
Application Number : 2267357
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 500UNIT/5ML
Packaging : 5ML
Brand Name : WILATE
Approval Date :
Application Number : 2286750
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 1000UNIT/10ML
Packaging : 10ML
Brand Name : WILATE
Approval Date :
Application Number : 2286769
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
COAGULATION FACTOR VII (HUMAN)
Dosage Form : KIT
Dosage Strength : 480UNIT/VIAL
Packaging : 20ML
Brand Name : OCTAPLEX
Approval Date :
Application Number : 2294664
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : KIT
Dosage Strength : 500UNIT/VIAL
Packaging : 20ML
Brand Name : OCTAPLEX
Approval Date :
Application Number : 2294664
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : KIT
Dosage Strength : 600UNIT/VIAL
Packaging : 20ML
Brand Name : OCTAPLEX
Approval Date :
Application Number : 2294664
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : KIT
Dosage Strength : 760UNIT/VIAL
Packaging : 20ML
Brand Name : OCTAPLEX
Approval Date :
Application Number : 2294664
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
COAGULATION FACTOR VII (HUMAN)
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 960UNIT/VIAL
Packaging : 40ML
Brand Name : OCTAPLEX
Approval Date :
Application Number : 2434970
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 1000UNIT/VIAL
Packaging : 40ML
Brand Name : OCTAPLEX
Approval Date :
Application Number : 2434970
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 1520UNIT/VIAL
Packaging : 40ML
Brand Name : OCTAPLEX
Approval Date :
Application Number : 2434970
Regulatory Info : Schedule D
Registration Country : Canada