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01 42Eli Lilly

02 1ORIFARM GROUP AS

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PharmaCompass

01

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : MOUNJARO (AUTOINJECTOR)

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 2.5MG/0.5ML (2.5MG/0.5ML)

Packaging :

Approval Date : 2022-05-13

Application Number : 215866

Regulatory Info : RX

Registration Country : USA

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02

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : MOUNJARO (AUTOINJECTOR)

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 5MG/0.5ML (5MG/0.5ML)

Packaging :

Approval Date : 2022-05-13

Application Number : 215866

Regulatory Info : RX

Registration Country : USA

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03

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : MOUNJARO (AUTOINJECTOR)

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 7.5MG/0.5ML (7.5MG/0.5ML)

Packaging :

Approval Date : 2022-05-13

Application Number : 215866

Regulatory Info : RX

Registration Country : USA

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04

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : MOUNJARO (AUTOINJECTOR)

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 10MG/0.5ML (10MG/0.5ML)

Packaging :

Approval Date : 2022-05-13

Application Number : 215866

Regulatory Info : RX

Registration Country : USA

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05

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : MOUNJARO (AUTOINJECTOR)

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 12.5MG/0.5ML (12.5MG/0.5ML)

Packaging :

Approval Date : 2022-05-13

Application Number : 215866

Regulatory Info : RX

Registration Country : USA

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06

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : MOUNJARO (AUTOINJECTOR)

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 15MG/0.5ML (15MG/0.5ML)

Packaging :

Approval Date : 2022-05-13

Application Number : 215866

Regulatory Info : RX

Registration Country : USA

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07

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : MOUNJARO

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 2.5MG/0.5ML (2.5MG/0.5ML)

Packaging :

Approval Date : 2023-07-28

Application Number : 215866

Regulatory Info : RX

Registration Country : USA

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08

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : MOUNJARO

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 5MG/0.5ML (5MG/0.5ML)

Packaging :

Approval Date : 2023-07-28

Application Number : 215866

Regulatory Info : RX

Registration Country : USA

blank

09

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : MOUNJARO

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 7.5MG/0.5ML (7.5MG/0.5ML)

Packaging :

Approval Date : 2023-07-28

Application Number : 215866

Regulatory Info : RX

Registration Country : USA

blank

10

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : MOUNJARO

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 10MG/0.5ML (10MG/0.5ML)

Packaging :

Approval Date : 2023-07-28

Application Number : 215866

Regulatory Info : RX

Registration Country : USA

blank

11

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : MOUNJARO

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 12.5MG/0.5ML (12.5MG/0.5ML)

Packaging :

Approval Date : 2023-07-28

Application Number : 215866

Regulatory Info : RX

Registration Country : USA

blank

12

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : MOUNJARO

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 15MG/0.5ML (15MG/0.5ML)

Packaging :

Approval Date : 2023-07-28

Application Number : 215866

Regulatory Info : RX

Registration Country : USA

blank

13

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : ZEPBOUND (AUTOINJECTOR)

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 2.5MG/0.5ML (2.5MG/0.5ML)

Packaging :

Approval Date : 2023-11-08

Application Number : 217806

Regulatory Info : RX

Registration Country : USA

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14

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : ZEPBOUND (AUTOINJECTOR)

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 5MG/0.5ML (5MG/0.5ML)

Packaging :

Approval Date : 2023-11-08

Application Number : 217806

Regulatory Info : RX

Registration Country : USA

blank

15

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : ZEPBOUND (AUTOINJECTOR)

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 7.5MG/0.5ML (7.5MG/0.5ML)

Packaging :

Approval Date : 2023-11-08

Application Number : 217806

Regulatory Info : RX

Registration Country : USA

blank

16

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : ZEPBOUND (AUTOINJECTOR)

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 10MG/0.5ML (10MG/0.5ML)

Packaging :

Approval Date : 2023-11-08

Application Number : 217806

Regulatory Info : RX

Registration Country : USA

blank

17

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : ZEPBOUND (AUTOINJECTOR)

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 12.5MG/0.5ML (12.5MG/0.5ML)

Packaging :

Approval Date : 2023-11-08

Application Number : 217806

Regulatory Info : RX

Registration Country : USA

blank

18

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : ZEPBOUND (AUTOINJECTOR)

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 15MG/0.5ML (15MG/0.5ML)

Packaging :

Approval Date : 2023-11-08

Application Number : 217806

Regulatory Info : RX

Registration Country : USA

blank

19

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : ZEPBOUND

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 2.5MG/0.5ML (2.5MG/0.5ML)

Packaging :

Approval Date : 2024-03-28

Application Number : 217806

Regulatory Info : RX

Registration Country : USA

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20

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

TIRZEPATIDE

Brand Name : ZEPBOUND

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 5MG/0.5ML (5MG/0.5ML)

Packaging :

Approval Date : 2024-03-28

Application Number : 217806

Regulatory Info : RX

Registration Country : USA

blank