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01 2Sanofi

02 12care4

03 2Accord healthcare

04 2Medical Valley

05 2Mepha Pharma

06 1ORIFARM GROUP AS

07 4Pfizer Inc

08 2STADA Arzneimittel

09 2Spirig Healthcare

10 2Viatris

11 2Zentiva

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Allowed

Registration Country : Switzerland

Fesoterodinum

Brand Name : Fesoterodin Zentiva

Dosage Form : Modified Release Tablet

Dosage Strength : 4mg

Packaging :

Approval Date : 31/03/2022

Application Number : 68694

Regulatory Info : Allowed

Registration Country : Switzerland

Sanofi Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Allowed

Registration Country : Switzerland

Fesoterodinum

Brand Name : Fesoterodin Zentiva

Dosage Form : Modified Release Tablet

Dosage Strength : 8mg

Packaging :

Approval Date : 31/03/2022

Application Number : 68694

Regulatory Info : Allowed

Registration Country : Switzerland

Sanofi Company Banner

03

BIO-Europe Spring
Not Confirmed
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BIO-Europe Spring
Not Confirmed

Fesoterodinfumarat

Brand Name : Fesoterodine Accord

Dosage Form : Tablet

Dosage Strength : 8mg

Packaging :

Approval Date : 26-08-2021

Application Number : 2.02E+13

Regulatory Info : Approved

Registration Country : Sweden

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04

BIO-Europe Spring
Not Confirmed
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BIO-Europe Spring
Not Confirmed

Fesoterodinfumarat

Brand Name : Fesoterodine Accord

Dosage Form : Tablet

Dosage Strength : 4mg

Packaging :

Approval Date : 26-10-2022

Application Number : 2.02E+13

Regulatory Info : Approved

Registration Country : Sweden

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05

BIO-Europe Spring
Not Confirmed
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BIO-Europe Spring
Not Confirmed

Fesoterodinfumarat

Brand Name : Fesoterodine Medical Valley

Dosage Form : Tablet

Dosage Strength : 4mg

Packaging :

Approval Date : 17-07-2022

Application Number : 2.02E+13

Regulatory Info : Approved

Registration Country : Sweden

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06

BIO-Europe Spring
Not Confirmed
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BIO-Europe Spring
Not Confirmed

Fesoterodinfumarat

Brand Name : Fesoterodine Medical Valley

Dosage Form : Tablet

Dosage Strength : 8mg

Packaging :

Approval Date : 17-07-2022

Application Number : 2.02E+13

Regulatory Info : Approved

Registration Country : Sweden

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07

BIO-Europe Spring
Not Confirmed
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BIO-Europe Spring
Not Confirmed

Fesoterodinum

Brand Name : Fesoterodin-Mepha

Dosage Form : Modified Release Tablet

Dosage Strength : 4mg

Packaging :

Approval Date : 27/06/2022

Application Number : 68790

Regulatory Info : Allowed

Registration Country : Switzerland

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08

BIO-Europe Spring
Not Confirmed
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arrow
BIO-Europe Spring
Not Confirmed

Fesoterodinum

Brand Name : Fesoterodin-Mepha

Dosage Form : Modified Release Tablet

Dosage Strength : 8mg

Packaging :

Approval Date : 27/06/2022

Application Number : 68790

Regulatory Info : Allowed

Registration Country : Switzerland

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09

BIO-Europe Spring
Not Confirmed
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arrow
BIO-Europe Spring
Not Confirmed

Fesoterodinum

Brand Name : Toviaz

Dosage Form : Tablet

Dosage Strength : 4mg

Packaging :

Approval Date : 18/12/2008

Application Number : 58743

Regulatory Info : Allowed

Registration Country : Switzerland

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10

BIO-Europe Spring
Not Confirmed
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BIO-Europe Spring
Not Confirmed

Fesoterodinum

Brand Name : Toviaz

Dosage Form : Tablet

Dosage Strength : 8mg

Packaging :

Approval Date : 18/12/2008

Application Number : 58743

Regulatory Info : Allowed

Registration Country : Switzerland

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11

BIO-Europe Spring
Not Confirmed
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BIO-Europe Spring
Not Confirmed

Fesoterodinfumarat

Brand Name : Toviaz

Dosage Form : Tablet

Dosage Strength : 4mg

Packaging :

Approval Date : 20-04-2007

Application Number : 2.01E+13

Regulatory Info : Approved

Registration Country : Sweden

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12

BIO-Europe Spring
Not Confirmed
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BIO-Europe Spring
Not Confirmed

Fesoterodinfumarat

Brand Name : Toviaz

Dosage Form : Tablet

Dosage Strength : 8mg

Packaging :

Approval Date : 20-04-2007

Application Number : 2.01E+13

Regulatory Info : Approved

Registration Country : Sweden

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13

BIO-Europe Spring
Not Confirmed
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BIO-Europe Spring
Not Confirmed

Fesoterodinum

Brand Name : Fesoterodin Spirig HC retard

Dosage Form : Modified Release Tablet

Dosage Strength : 4mg

Packaging :

Approval Date : 05/09/2024

Application Number : 69550

Regulatory Info : Allowed

Registration Country : Switzerland

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14

BIO-Europe Spring
Not Confirmed
arrow
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BIO-Europe Spring
Not Confirmed

Fesoterodinum

Brand Name : Fesoterodin Spirig HC retard

Dosage Form : Modified Release Tablet

Dosage Strength : 8mg

Packaging :

Approval Date : 05/09/2024

Application Number : 69550

Regulatory Info : Allowed

Registration Country : Switzerland

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15

BIO-Europe Spring
Not Confirmed
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BIO-Europe Spring
Not Confirmed

Fesoterodinfumarat

Brand Name : Fesoterodine Stada

Dosage Form : Tablet

Dosage Strength : 4mg

Packaging :

Approval Date : 19-04-2021

Application Number : 2.02E+13

Regulatory Info : Approved

Registration Country : Sweden

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16

BIO-Europe Spring
Not Confirmed
arrow
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BIO-Europe Spring
Not Confirmed

Fesoterodinfumarat

Brand Name : Fesoterodine Stada

Dosage Form : Tablet

Dosage Strength : 8mg

Packaging :

Approval Date : 19-04-2021

Application Number : 2.02E+13

Regulatory Info : Approved

Registration Country : Sweden

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17

BIO-Europe Spring
Not Confirmed
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BIO-Europe Spring
Not Confirmed

Fesoterodine

Brand Name : Fesoterodine Viatris

Dosage Form : Prolonged-Release Tablet

Dosage Strength : 3.1MG

Packaging :

Approval Date : 2024-08-02

Application Number :

Regulatory Info : Authorised

Registration Country : Malta

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18

BIO-Europe Spring
Not Confirmed
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BIO-Europe Spring
Not Confirmed

Fesoterodine

Brand Name : Fesoterodine Viatris

Dosage Form : Prolonged-Release Tablet

Dosage Strength : 6.2MG

Packaging :

Approval Date : 2024-08-02

Application Number :

Regulatory Info : Authorised

Registration Country : Malta

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19

BIO-Europe Spring
Not Confirmed
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BIO-Europe Spring
Not Confirmed

Fesoterodinfumarat

Brand Name : Fesoterodine Zentiva

Dosage Form : Tablet

Dosage Strength : 4mg

Packaging :

Approval Date : 06-02-2023

Application Number : 2.02E+13

Regulatory Info : Approved

Registration Country : Sweden

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20

BIO-Europe Spring
Not Confirmed
arrow
arrow
BIO-Europe Spring
Not Confirmed

Fesoterodinfumarat

Brand Name : Fesoterodine Zentiva

Dosage Form : Tablet

Dosage Strength : 8mg

Packaging :

Approval Date : 06-02-2023

Application Number : 2.02E+13

Regulatory Info : Approved

Registration Country : Sweden

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