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01 1Dong Bang Co., Ltd
02 4Ferring Pharmaceuticals
03 1PARNELL TECHNOLOGIES PTY LTD
04 1VETOQUINOL N A INC
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01 2INJECTABLE;INJECTION
02 1Injectable
03 2SOLUTION
04 2Solution For Injection
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01 2DISCN
02 2Deregistered
03 2Prescription
04 1Blank
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01 1FERTILINE
02 1GONABREED
03 1Gonadon
04 2LUTREPULSE KIT
05 2Lutrelef
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01 2Canada
02 1South Korea
03 2Sweden
04 2USA
Regulatory Info :
Registration Country : South Korea
Brand Name : Gonadon
Dosage Form : Injectable
Dosage Strength : 100MCG/ML
Packaging : 10ML, 20ML Vials
Approval Date :
Application Number :
Regulatory Info :
Registration Country : South Korea
Regulatory Info : DISCN
Registration Country : USA
Brand Name : LUTREPULSE KIT
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 0.8MG/VIAL
Packaging :
Approval Date : 1989-10-10
Application Number : 19687
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : LUTREPULSE KIT
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 3.2MG/VIAL
Packaging :
Approval Date : 1989-10-10
Application Number : 19687
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Lutrelef
Dosage Form : Solution For Injection
Dosage Strength : 0.8mg
Packaging :
Approval Date : 12/06/1987
Application Number : 19870612000037
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Lutrelef
Dosage Form : Solution For Injection
Dosage Strength : 3.2mg
Packaging :
Approval Date : 12/06/1987
Application Number : 19870612000044
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : GONABREED
Dosage Form : SOLUTION
Dosage Strength : 100MCG/ML
Packaging :
Approval Date :
Application Number : 2496763
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : FERTILINE
Dosage Form : SOLUTION
Dosage Strength : 50MCG/ML
Packaging : 20/50 ML
Approval Date :
Application Number : 2030314
Regulatory Info : Prescription
Registration Country : Canada