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01 8Sanofi

02 1Biocon

03 1Biocon Biologics

04 2Biosimilar Collaborations Ireland Limited

05 88Novo Nordisk

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Approved

Registration Country : Sweden

Insulin, Aspart

Brand Name : Insulin Aspart Sanofi

Dosage Form : Injectable Solution

Dosage Strength : 100E/ml

Packaging :

Approval Date : 21/04/2021

Application Number : 20200727000046

Regulatory Info : Approved

Registration Country : Sweden

Sanofi Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Approved

Registration Country : Sweden

Insulin, Aspart

Brand Name : Insulin Aspart Sanofi

Dosage Form : Solution For Injection

Dosage Strength : 100E/ml

Packaging :

Approval Date : 25/06/2020

Application Number : 20190604000057

Regulatory Info : Approved

Registration Country : Sweden

Sanofi Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Approved

Registration Country : Sweden

Insulin, Aspart

Brand Name : Insulin Aspart Sanofi

Dosage Form : Solution For Injection

Dosage Strength : 100E/ml

Packaging :

Approval Date : 25/06/2020

Application Number : 20190604000064

Regulatory Info : Approved

Registration Country : Sweden

Sanofi Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Deregistered

Registration Country : Sweden

Insulin Aspart (Soluble); Insulin Aspart Protamine

Brand Name : Truvelog Mix 30

Dosage Form : Suspension For Injection

Dosage Strength : 100E/ml

Packaging :

Approval Date : 25/04/2022

Application Number : 20210429000121

Regulatory Info : Deregistered

Registration Country : Sweden

Sanofi Company Banner

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Deregistered

Registration Country : Sweden

Insulin Aspart (Soluble); Insulin Aspart Protamine

Brand Name : Truvelog Mix 30

Dosage Form : Injectable Solution

Dosage Strength : 100E/ml

Packaging :

Approval Date : 25/04/2022

Application Number : 20210429000114

Regulatory Info : Deregistered

Registration Country : Sweden

Sanofi Company Banner

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Schedule D

Registration Country : Canada

INSULIN ASPART

Brand Name : TRURAPI

Dosage Form : SOLUTION

Dosage Strength : 100UNIT/ML

Packaging :

Approval Date :

Application Number : 2506564

Regulatory Info : Schedule D

Registration Country : Canada

Sanofi Company Banner

07

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Schedule D

Registration Country : Canada

INSULIN ASPART

Brand Name : TRURAPI

Dosage Form : SOLUTION

Dosage Strength : 100UNIT/ML

Packaging :

Approval Date :

Application Number : 2506572

Regulatory Info : Schedule D

Registration Country : Canada

Sanofi Company Banner

08

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Schedule D

Registration Country : Canada

INSULIN ASPART

Brand Name : TRURAPI

Dosage Form : SOLUTION

Dosage Strength : 100UNIT/ML

Packaging :

Approval Date :

Application Number : 2529254

Regulatory Info : Schedule D

Registration Country : Canada

Sanofi Company Banner

09

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

INSULIN ASPART RECOMBINANT

Brand Name : NOVOLOG

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 1000 UNITS/10ML (100 UNITS/ML)

Packaging :

Approval Date :

Application Number : 20986

Regulatory Info :

Registration Country : USA

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10

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

INSULIN ASPART RECOMBINANT

Brand Name : NOVOLOG PENFILL

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 300 UNITS/3ML (100 UNITS/ML)

Packaging :

Approval Date :

Application Number : 20986

Regulatory Info :

Registration Country : USA

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11

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

INSULIN ASPART RECOMBINANT

Brand Name : NOVOLOG FLEXPEN

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 300 UNITS/3ML (100 UNITS/ML)

Packaging :

Approval Date :

Application Number : 20986

Regulatory Info :

Registration Country : USA

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12

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

INSULIN ASPART RECOMBINANT

Brand Name : NOVOLOG INNOLET

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 300 UNITS/3ML (100 UNITS/ML)

Packaging :

Approval Date :

Application Number : 20986

Regulatory Info :

Registration Country : USA

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13

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

INSULIN ASPART RECOMBINANT

Brand Name : NOVOLOG FLEXTOUCH

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 300 UNITS/3ML (100 UNITS/ML)

Packaging :

Approval Date :

Application Number : 20986

Regulatory Info :

Registration Country : USA

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14

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

INSULIN ASPART PROTAMINE RECOMBINANT; INSULIN ASPART RECOMBINANT

Brand Name : NOVOLOG MIX 70/30

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 700 UNITS/10ML; 300 UNITS/10ML (70 UNITS/ML; 30 UNITS/ML)

Packaging :

Approval Date :

Application Number : 21172

Regulatory Info :

Registration Country : USA

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15

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

INSULIN ASPART PROTAMINE RECOMBINANT; INSULIN ASPART RECOMBINANT

Brand Name : NOVOLOG MIX 70/30 PENFILL

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 210 UNITS/3ML;90 UNITS/3ML (70 UNITS/ML; 30 UNITS/ML)

Packaging :

Approval Date :

Application Number : 21172

Regulatory Info :

Registration Country : USA

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16

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

INSULIN ASPART PROTAMINE RECOMBINANT; INSULIN ASPART RECOMBINANT

Brand Name : NOVOLOG MIX 70/30 PENFILL

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 210 UNITS/3ML;90 UNITS/3ML (70 UNITS/ML; 30 UNITS/ML)

Packaging :

Approval Date :

Application Number : 21172

Regulatory Info :

Registration Country : USA

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17

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

INSULIN ASPART PROTAMINE RECOMBINANT; INSULIN ASPART RECOMBINANT

Brand Name : NOVOLOG MIX 70/30 FLEXPEN

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 210 UNITS/3ML; 90 UNITS/3ML (70 UNITS/ML; 30 UNITS/ML)

Packaging :

Approval Date :

Application Number : 21172

Regulatory Info :

Registration Country : USA

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18

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

INSULIN ASPART PROTAMINE RECOMBINANT; INSULIN ASPART RECOMBINANT

Brand Name : NOVOLOG MIX 50/50

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 50 UNITS/ML;50 UNITS/ML

Packaging :

Approval Date :

Application Number : 21810

Regulatory Info :

Registration Country : USA

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19

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

INSULIN ASPART; INSULIN DEGLUDEC

Brand Name : RYZODEG 70/30

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 90 UNITS/3ML;210 UNITS/3ML (30 UNITS/ML;70 UNITS/ML)

Packaging :

Approval Date :

Application Number : 203313

Regulatory Info :

Registration Country : USA

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20

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

INSULIN ASPART

Brand Name : FIASP

Dosage Form : SOLUTION;INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : 1000 UNITS/10ML (100 UNITS/ML)

Packaging :

Approval Date :

Application Number : 208751

Regulatory Info :

Registration Country : USA

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