01 4ANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, B-DOMAIN TRUNCATED), PEGYLATED
02 1CATRIDECACOG
03 4COAGULATION FACTOR IX (RECOMBINANT), PEGYLATED
04 3EPTACOG ALFA (ACTIVATED)
05 2ESTRADIOL
06 1ESTRADIOL (ESTRADIOL HEMIHYDRATE)
07 2GLUCAGON (RECOMBINANT DNA ORIGIN) (GLUCAGON HYDROCHLORIDE)
08 6INSULIN ASPART
09 1INSULIN ASPART PROTAMINE
10 4INSULIN DEGLUDEC
11 1INSULIN DETEMIR
12 3INSULIN ICODEC
13 4INSULIN INJECTION HUMAN BIOSYNTHETIC
14 4INSULIN ISOPHANE HUMAN BIOSYNTHETIC
15 3LIRAGLUTIDE
16 2NORETHINDRONE ACETATE
17 3REPAGLINIDE
18 11SEMAGLUTIDE
19 3SOMAPACITAN
20 6SOMATROPIN
21 6TUROCTOCOG ALFA
01 11KIT
02 9POWDER FOR SOLUTION
03 35SOLUTION
04 8SUSPENSION
05 10TABLET
06 1VAGINAL TABLET
01 10.1MG
02 30.5MG
03 10.68MG/ML
04 11.34MG/ML
05 31000UNIT/VIAL
06 13100UNIT/ML
07 11050UNIT/1.5ML
08 110MCG
09 310MG/1.5ML
10 114MG
11 11500UNIT/VIAL
12 315MG/1.5ML
13 21MG
14 11MG/1.5ML
15 11MG/ACT
16 31MG/VIAL
17 32000UNIT/VIAL
18 1200UNIT/ML
19 12100UNIT/3ML
20 12500UNIT/VIAL
21 1250UNIT/VIAL
22 12MG
23 12MG/1.5ML
24 12MG/VIAL
25 13.6MG/ML
26 33000UNIT/VIAL
27 330UNIT/ML
28 13MG
29 14MG/3ML
30 3500UNIT/VIAL
31 35MG/1.5ML
32 15MG/VIAL
33 16.8MG/3ML
34 26MG/ML
35 1700UNIT/ML
36 370UNIT/ML
37 17MG
38 19.6MG/3ML
01 2ACTIVELLE
02 2ACTIVELLE LD
03 3AWIQLI
04 4ESPEROCT
05 3FIASP
06 1GLUCAGEN
07 1GLUCAGEN HYPOKIT
08 1GLUCONORM 0.5MG
09 1GLUCONORM 1.0MG
10 1GLUCONORM 2.0MG
11 1LEVEMIR PENFILL
12 3NIASTASE RT
13 3NORDITROPIN FLEXPRO
14 3NORDITROPIN NORDIFLEX
15 2NOVOLIN GE 30/70
16 2NOVOLIN GE 30/70 PENFILL
17 1NOVOLIN GE NPH
18 1NOVOLIN GE NPH PENFILL
19 1NOVOLIN GE TORONTO
20 1NOVOLIN GE TORONTO PENFILL
21 2NOVOMIX 30
22 2NOVORAPID
23 3OZEMPIC
24 4REBINYN
25 3RYBELSUS
26 1SAXENDA
27 3SOGROYA
28 3TRESIBA
29 1TRETTEN
30 1VAGIFEM 10
31 1VICTOZA
32 5WEGOVY
33 2XULTOPHY
34 6ZONOVATE
Regulatory Info : Schedule D
Registration Country : Canada
ANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, B-DOMAIN ...
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 500UNIT/VIAL
Packaging :
Brand Name : ESPEROCT
Approval Date :
Application Number : 2490064
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
ANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, B-DOMAIN ...
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 1000UNIT/VIAL
Packaging :
Brand Name : ESPEROCT
Approval Date :
Application Number : 2490072
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
ANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, B-DOMAIN ...
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 2000UNIT/VIAL
Packaging :
Brand Name : ESPEROCT
Approval Date :
Application Number : 2490099
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
ANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, B-DOMAIN ...
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 3000UNIT/VIAL
Packaging :
Brand Name : ESPEROCT
Approval Date :
Application Number : 2490102
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : KIT
Dosage Strength : 1MG/VIAL
Packaging :
Brand Name : NIASTASE RT
Approval Date :
Application Number : 2417103
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 2500UNIT/VIAL
Packaging : 2500IU
Brand Name : TRETTEN
Approval Date :
Application Number : 2389975
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
COAGULATION FACTOR IX (RECOMBINANT), PEGYLATED
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 3000UNIT/VIAL
Packaging :
Brand Name : REBINYN
Approval Date :
Application Number : 2532964
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
COAGULATION FACTOR IX (RECOMBINANT), PEGYLATED
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 500UNIT/VIAL
Packaging : 500 IU VIAL
Brand Name : REBINYN
Approval Date :
Application Number : 2470187
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
COAGULATION FACTOR IX (RECOMBINANT), PEGYLATED
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 1000UNIT/VIAL
Packaging : 1000 IU VIAL
Brand Name : REBINYN
Approval Date :
Application Number : 2470268
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
COAGULATION FACTOR IX (RECOMBINANT), PEGYLATED
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 2000UNIT/VIAL
Packaging : 2000 IU VIAL
Brand Name : REBINYN
Approval Date :
Application Number : 2470276
Regulatory Info : Schedule D
Registration Country : Canada
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