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01 1Alfuzosinhydroklorid
02 3Anastrozole
03 2Bicalutamide
04 3Budesonide; Formoterol Fumarate Dihydrate
05 2Budesonide; Formoterol Fumarate Dihydrate
06 3Cyclosporine
07 1Dalteparin Sodium
08 1Donepezil Hydrochloride, Anhydrous
09 2Estradiol Hemihydrate
10 1Felodipine; Metoprolol Succinate
11 3Goserelin Acetate
12 1Isradipine
13 1Kandesartancilexetil
14 1Latanoprost; Timolol Maleate
15 1Meropenem Trihydrate
16 1Omeprazol
17 1Propranolol Hydrochloride
18 2Quetiapine Fumarate
19 1Ticlopidine Hydrochloride
20 2Topiramate
21 3Venlafaxinhydroklorid
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01 36Qdoxx Pharma Ab
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01 7Capsule
02 1Eye Drop
03 10Film Coated Tablet
04 3Implant In Pre-Filled Syringe
05 5Inhalation Powder
06 1Injectable Solution
07 1Injection/Infusion Solution
08 6Tablet
09 2Vaginal Tablet
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01 310.8mg
02 110000IU/ml
03 3100mg
04 110mg
05 2150mg
06 2160mcg/dose;4.5mcg/dose
07 12.5mg
08 2200mg
09 120mg
10 1250mg
11 225mcg
12 125mg
13 2320mcg/dose;9mcg/dose
14 137.5mg
15 14mg
16 250mg
17 15mg
18 15mg;50mg
19 175mg
20 180mcg/4.5mcg/inhalation
21 180mg
22 5Blank
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01 36Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Tablet
Brand Name : Xatral Od
Dosage Strength : 10mg
Packaging :
Approval Date : 06/12/2006
Application Number : 20060211000156
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Arimidex
Dosage Strength :
Packaging :
Approval Date : 30/06/2006
Application Number : 20051215000419
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Arimidex
Dosage Strength :
Packaging :
Approval Date : 29/08/2007
Application Number : 20070221000015
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Arimidex
Dosage Strength :
Packaging :
Approval Date : 29/02/2008
Application Number : 20071025000041
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Casodex
Dosage Strength : 150mg
Packaging :
Approval Date : 20/12/2007
Application Number : 20070124000044
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Casodex
Dosage Strength : 50mg
Packaging :
Approval Date : 20/12/2007
Application Number : 20070124000037
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Budesonide; Formoterol Fumarate Dihydrate
Dosage Form : Inhalation Powder
Brand Name : Symbicort Turbohaler
Dosage Strength : 160mcg/dose;4.5mcg/dos...
Packaging :
Approval Date : 21/05/2007
Application Number : 20060713000074
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Budesonide; Formoterol Fumarate Dihydrate
Dosage Form : Inhalation Powder
Brand Name : Symbicort Turbohaler
Dosage Strength : 160mcg/dose;4.5mcg/dos...
Packaging :
Approval Date : 21/05/2007
Application Number : 20060710000244
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Budesonide; Formoterol Fumarate Dihydrate
Dosage Form : Inhalation Powder
Brand Name : Symbicort Mite Turbuhaler
Dosage Strength : 80mcg/4.5mcg/inhalatio...
Packaging :
Approval Date : 17/11/2005
Application Number : 20050526000019
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Budesonide; Formoterol Fumarate Dihydrate
Dosage Form : Inhalation Powder
Brand Name : Symbicort Forte Turbohale...
Dosage Strength : 320mcg/dose;9mcg/dose
Packaging :
Approval Date : 21/05/2007
Application Number : 20060718000017
Regulatory Info : Deregistered
Registration Country : Sweden