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01 8Pfizer Consumer Healthcare
02 21Pfizer Inc
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01 5INJECTABLE;SUBCUTANEOUS
02 5POWDER FOR SOLUTION
03 6Powder And Solvent For Injectable Solution
04 5Solution For Injection
05 8Blank
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01 5Approved
02 6Authorized
03 3Prescription
04 2Schedule D
05 13Blank
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01 10SOMAVERT
02 19Somavert
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01 8Australia
02 5Canada
03 6Spain
04 5Sweden
05 5USA
Regulatory Info :
Registration Country : Australia
Brand Name : Somavert
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Somavert
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Somavert
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Somavert
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Somavert
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : USA
Brand Name : SOMAVERT
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 10MG/VIAL
Packaging :
Approval Date :
Application Number : 21106
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : SOMAVERT
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 15MG/VIAL
Packaging :
Approval Date :
Application Number : 21106
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : SOMAVERT
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 20MG/VIAL
Packaging :
Approval Date :
Application Number : 21106
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : SOMAVERT
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 25MG/VIAL
Packaging :
Approval Date :
Application Number : 21106
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : SOMAVERT
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 30MG/VIAL
Packaging :
Approval Date :
Application Number : 21106
Regulatory Info :
Registration Country : USA
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Somavert
Dosage Form : Solution For Injection
Dosage Strength : 10mg
Packaging :
Approval Date : 13/11/2002
Application Number : 20021113000019
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Somavert
Dosage Form : Solution For Injection
Dosage Strength : 15mg
Packaging :
Approval Date : 13/11/2002
Application Number : 20021113000026
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Somavert
Dosage Form : Solution For Injection
Dosage Strength : 20mg
Packaging :
Approval Date : 13/11/2002
Application Number : 20021113000033
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Somavert
Dosage Form : Solution For Injection
Dosage Strength : 25mg
Packaging :
Approval Date : 17/07/2015
Application Number : 20140507000012
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Somavert
Dosage Form : Solution For Injection
Dosage Strength : 30mg
Packaging :
Approval Date : 17/07/2015
Application Number : 20140507000029
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Schedule D
Registration Country : Canada
Brand Name : SOMAVERT
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 10MG/VIAL
Packaging : 8ML
Approval Date :
Application Number : 2272199
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : SOMAVERT
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 15MG/VIAL
Packaging : 8ML
Approval Date :
Application Number : 2272202
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : SOMAVERT
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 20MG/VIAL
Packaging : 8ML
Approval Date :
Application Number : 2272210
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : SOMAVERT
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 25MG/VIAL
Packaging : 8ML
Approval Date :
Application Number : 2448831
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Brand Name : SOMAVERT
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 30MG/VIAL
Packaging : 8ML
Approval Date :
Application Number : 2448858
Regulatory Info : Schedule D
Registration Country : Canada