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01 32Eli Lilly
02 1ORIFARM GROUP AS
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01 6SOLUTION
02 24SOLUTION;SUBCUTANEOUS
03 1Solution for injection
04 2Solution for injection in a pre-filled pen
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01 24RX
02 9Blank
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01 12MOUNJARO
02 6MOUNJARO (AUTOINJECTOR)
03 3Mounjaro
04 6ZEPBOUND
05 6ZEPBOUND (AUTOINJECTOR)
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01 6Canada
02 3Norway
03 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
Regulatory Info : RX
Registration Country : USA
Brand Name : ZEPBOUND
Dosage Form : SOLUTION;SUBCUTANEOUS
Dosage Strength : 7.5MG/0.5ML (7.5MG/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 : 10MG/0.5ML (10MG/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 : 12.5MG/0.5ML (12.5MG/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 : 15MG/0.5ML (15MG/0.5ML)
Packaging :
Approval Date : 2024-03-28
Application Number : 217806
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Norway
Brand Name : Mounjaro
Dosage Form : Solution for injection in a pre-filled pen
Dosage Strength : 2.5 mg
Packaging : Pre-filled pen 4 0.5ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Brand Name : Mounjaro
Dosage Form : Solution for injection in a pre-filled pen
Dosage Strength : 5 mg
Packaging : Pre-filled pen 4 0.5ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Canada
Brand Name : MOUNJARO
Dosage Form : SOLUTION
Dosage Strength : 2.5MG/0.5ML
Packaging :
Approval Date :
Application Number : 2541041
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
Brand Name : MOUNJARO
Dosage Form : SOLUTION
Dosage Strength : 5MG/0.5ML
Packaging :
Approval Date :
Application Number : 2541068
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
Brand Name : MOUNJARO
Dosage Form : SOLUTION
Dosage Strength : 7.5MG/0.5ML
Packaging :
Approval Date :
Application Number : 2541076
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Norway
Brand Name : Mounjaro
Dosage Form : Solution for injection
Dosage Strength : 2.5 mg
Packaging : Vials 1 0.5ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway