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01 78Eli Lilly
02 1ORIFARM GROUP AS
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01 4INJ
02 6Injectable Solution
03 4Injectable Solution In A Pre-Filled Pen
04 2Injectable Solution In Pre-Filled Pen
05 12SOLUTION
06 24SOLUTION;SUBCUTANEOUS
07 24Solution For Injection
08 1Solution for injection
09 2Solution for injection in a pre-filled pen
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01 18Allowed
02 18Approved
03 4Originator
04 24RX
05 15Blank
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01 12MOUNJARO
02 6MOUNJARO (AUTOINJECTOR)
03 6MOUNJARO KWIKPEN
04 27Mounjaro
05 1Mounjaro 10mg
06 1Mounjaro 2,5mg
07 1Mounjaro 5mg
08 1Mounjaro 7,5mg
09 6Mounjaro KwikPen
10 6Mounjaro Kwikpen
11 6ZEPBOUND
12 6ZEPBOUND (AUTOINJECTOR)
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01 12Canada
02 3Norway
03 4South Africa
04 18Sweden
05 18Switzerland
06 24USA
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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