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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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PharmaCompass

01

Brand Name : Xatral Od

ESF Europe
Not Confirmed
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Brand Name : Xatral Od

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ESF Europe
Not Confirmed

Oasmia Pharmaceutical

Dosage Form : Tablet

Brand Name : Xatral Od

Dosage Strength : 10mg

Packaging :

Approval Date : 06-12-2006

Application Number : 2.01E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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02

Brand Name : Arimidex

ESF Europe
Not Confirmed
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Brand Name : Arimidex

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ESF Europe
Not Confirmed

Oasmia Pharmaceutical

Dosage Form : Film Coated Tablet

Brand Name : Arimidex

Dosage Strength :

Packaging :

Approval Date : 30-06-2006

Application Number : 2.01E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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03

Brand Name : Arimidex

ESF Europe
Not Confirmed
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Brand Name : Arimidex

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ESF Europe
Not Confirmed

Oasmia Pharmaceutical

Dosage Form : Film Coated Tablet

Brand Name : Arimidex

Dosage Strength :

Packaging :

Approval Date : 29-08-2007

Application Number : 2.01E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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04

Brand Name : Arimidex

ESF Europe
Not Confirmed
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Brand Name : Arimidex

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ESF Europe
Not Confirmed

Oasmia Pharmaceutical

Dosage Form : Film Coated Tablet

Brand Name : Arimidex

Dosage Strength :

Packaging :

Approval Date : 29-02-2008

Application Number : 2.01E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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05

Brand Name : Casodex

ESF Europe
Not Confirmed
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Brand Name : Casodex

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ESF Europe
Not Confirmed

Oasmia Pharmaceutical

Dosage Form : Film Coated Tablet

Brand Name : Casodex

Dosage Strength : 50mg

Packaging :

Approval Date : 20-12-2007

Application Number : 2.01E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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06

Brand Name : Casodex

ESF Europe
Not Confirmed
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Brand Name : Casodex

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ESF Europe
Not Confirmed

Oasmia Pharmaceutical

Dosage Form : Film Coated Tablet

Brand Name : Casodex

Dosage Strength : 150mg

Packaging :

Approval Date : 20-12-2007

Application Number : 2.01E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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07

Brand Name : Symbicort Mite Turbu...

ESF Europe
Not Confirmed
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Brand Name : Symbicort Mite Turbu...

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ESF Europe
Not Confirmed

Oasmia Pharmaceutical

Dosage Form : Inhalation Powder

Brand Name : Symbicort Mite Turbuhaler

Dosage Strength : 80mcg/4.5mcg/inhalatio...

Packaging :

Approval Date : 17-11-2005

Application Number : 2.01E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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08

Brand Name : Symbicort Turbohaler

ESF Europe
Not Confirmed
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Brand Name : Symbicort Turbohaler

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ESF Europe
Not Confirmed

Oasmia Pharmaceutical

Dosage Form : Inhalation Powder

Brand Name : Symbicort Turbohaler

Dosage Strength : 160mcg/dose;4.5mcg/dos...

Packaging :

Approval Date : 21-05-2007

Application Number : 2.01E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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09

Brand Name : Symbicort Forte Turb...

ESF Europe
Not Confirmed
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Brand Name : Symbicort Forte Turb...

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ESF Europe
Not Confirmed

Oasmia Pharmaceutical

Dosage Form : Inhalation Powder

Brand Name : Symbicort Forte Turbohale...

Dosage Strength : 320mcg/dose;9mcg/dose

Packaging :

Approval Date : 21-05-2007

Application Number : 2.01E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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10

Brand Name : Symbicort Turbohaler

ESF Europe
Not Confirmed
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Brand Name : Symbicort Turbohaler

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ESF Europe
Not Confirmed

Oasmia Pharmaceutical

Dosage Form : Inhalation Powder

Brand Name : Symbicort Turbohaler

Dosage Strength : 160mcg/dose;4.5mcg/dos...

Packaging :

Approval Date : 21-05-2007

Application Number : 2.01E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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