Omgene: R&D-based biopharmaceutical company with GMP facilities, focused on innovation and high-quality, affordable medicines.
01 2Omgene Life Sciences Pvt. Ltd
02 2Accord healthcare
03 1CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD.
04 18Ferring Pharmaceuticals
01 1Degarelix 120Mg 2 Units Parenteral Use
02 1Degarelix 80Mg 1 Unit Parenteral Use
03 2Injection
04 1NJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
05 2POI
06 2POWDER FOR SOLUTION
07 2POWDER;SUBCUTANEOUS
08 2Powder And Solvent For Injectable Solution
09 2Powder For Injection
10 2Powder and liquid to the injection fluid, resolution
11 4Solution For Injection
12 2Blank
01 2Allowed
02 4Approved
03 2Authorized
04 2Originator
05 2Prescription
06 2RX
07 9Blank
01 2Company
02 1DEGARELIX ACETATE
03 2Degarelix Accord
04 2Degarelix Acetate
05 4FIRMAGON
06 2Firm Agon
07 6Firmagon
08 1Firmagon 120 Mg
09 1Firmagon 120mg
10 1Firmagon 80 Mg
11 1Firmagon 80mg
01 2Australia
02 2Canada
03 2India
04 2Italy
05 2Norway
06 2South Africa
07 2Spain
08 4Sweden
09 2Switzerland
10 3USA
Omgene: R&D-based biopharmaceutical company with GMP facilities, focused on innovation and high-quality, affordable medicines.
Regulatory Info :
Registration Country : India
Brand Name : Degarelix Acetate
Dosage Form : Injection
Dosage Strength : 80MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Omgene: R&D-based biopharmaceutical company with GMP facilities, focused on innovation and high-quality, affordable medicines.
Regulatory Info :
Registration Country : India
Brand Name : Degarelix Acetate
Dosage Form : Injection
Dosage Strength : 120MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Degarelix Accord
Dosage Form : Solution For Injection
Dosage Strength : 120mg
Packaging :
Approval Date : 29/09/2023
Application Number : 20220627000151
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Degarelix Accord
Dosage Form : Solution For Injection
Dosage Strength : 80mg
Packaging :
Approval Date : 29/09/2023
Application Number : 20220627000144
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : RX
Registration Country : USA
Brand Name : FIRMAGON
Dosage Form : POWDER;SUBCUTANEOUS
Dosage Strength : EQ 80MG BASE/VIAL
Packaging :
Approval Date : 2008-12-24
Application Number : 22201
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FIRMAGON
Dosage Form : POWDER;SUBCUTANEOUS
Dosage Strength : EQ 120MG BASE/VIAL
Packaging :
Approval Date : 2008-12-24
Application Number : 22201
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Italy
Brand Name : Firmagon
Dosage Form : Degarelix 120Mg 2 Units Parenteral Use
Dosage Strength : 2 vials groun 120 mg + 2 Syringes solv 3 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Firmagon
Dosage Form : Degarelix 80Mg 1 Unit Parenteral Use
Dosage Strength : 1 vial 80 mg groun + 1 syringe solv 4,2 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
Brand Name : Firm Agon
Dosage Form : Powder and liquid to the injection fluid, resolution
Dosage Strength : 120 mg
Packaging : Hood glass
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Brand Name : Firm Agon
Dosage Form : Powder and liquid to the injection fluid, resolution
Dosage Strength : 80 mg
Packaging : Hood glass
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Company
Dosage Form : Solution For Injection
Dosage Strength : 120mg
Packaging :
Approval Date : 17/02/2009
Application Number : 20080417000026
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Company
Dosage Form : Solution For Injection
Dosage Strength : 80mg
Packaging :
Approval Date : 17/02/2009
Application Number : 20080417000019
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Firmagon
Dosage Form : Powder For Injection
Dosage Strength : 80mg
Packaging :
Approval Date : 12/02/2010
Application Number : 59455
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Firmagon
Dosage Form : Powder For Injection
Dosage Strength : 120mg
Packaging :
Approval Date : 12/02/2010
Application Number : 59455
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : FIRMAGON
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 80MG/VIAL
Packaging : 80MG
Approval Date :
Application Number : 2337029
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : FIRMAGON
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 120MG/VIAL
Packaging : 120MG
Approval Date :
Application Number : 2337037
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Firmagon 120 Mg
Dosage Form : POI
Dosage Strength : 120mg
Packaging : 3X2mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Firmagon 80 Mg
Dosage Form : POI
Dosage Strength : 80mg
Packaging : 4.2X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info :
Registration Country : Australia
Brand Name : Firmagon 80mg
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : USA
Brand Name : DEGARELIX ACETATE
Dosage Form : NJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Dosage Strength : 80MG
Packaging :
Approval Date :
Application Number : 215791
Regulatory Info :
Registration Country : USA
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