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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

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PharmaCompass

01

Brand Name : ESPEROCT

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : ESPEROCT

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Pharma, Lab & Chemical Expo
Not Confirmed

Novo Nordisk

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

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02

Brand Name : ESPEROCT

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : ESPEROCT

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Pharma, Lab & Chemical Expo
Not Confirmed

Novo Nordisk

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

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03

Brand Name : ESPEROCT

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : ESPEROCT

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Pharma, Lab & Chemical Expo
Not Confirmed

Novo Nordisk

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

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04

Brand Name : ESPEROCT

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : ESPEROCT

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Pharma, Lab & Chemical Expo
Not Confirmed

Novo Nordisk

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

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05

Brand Name : NIASTASE RT

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : NIASTASE RT

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Pharma, Lab & Chemical Expo
Not Confirmed

Novo Nordisk

Dosage Form : KIT

Dosage Strength : 1MG/VIAL

Packaging :

Brand Name : NIASTASE RT

Approval Date :

Application Number : 2417103

Regulatory Info : Schedule D

Registration Country : Canada

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06

Brand Name : TRETTEN

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : TRETTEN

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Pharma, Lab & Chemical Expo
Not Confirmed

Novo Nordisk

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

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07

Brand Name : REBINYN

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : REBINYN

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Pharma, Lab & Chemical Expo
Not Confirmed

Novo Nordisk

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

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08

Brand Name : REBINYN

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : REBINYN

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Pharma, Lab & Chemical Expo
Not Confirmed

Novo Nordisk

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

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09

Brand Name : REBINYN

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : REBINYN

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Pharma, Lab & Chemical Expo
Not Confirmed

Novo Nordisk

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

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10

Brand Name : REBINYN

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : REBINYN

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Pharma, Lab & Chemical Expo
Not Confirmed

Novo Nordisk

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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Novo Nordisk is a supplier offers 20 products (APIs, Excipients or Intermediates).

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