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01 1SANOFI-AVENTIS SpA

02 1Sanofi Malta Limited

03 1Sanofi-Synthelabo Ab

04 22Care4 Aps

05 2Accord Healthcare Bv

06 4Central Procurement & Supplies Unit

07 1Cheplapharm Arzneimittel Gmbh

08 1Cherubino Limited

09 1EG SpA

10 1Ebb Medical Ab

11 1Farco Pharma Gmbh

12 1Health House Pharma Ltd T/As P&D Pharmaceuticals Ltd

13 3Janssen-Cilag Ab

14 1MYLAN SpA

15 1Medartuum Ab

16 1Medice Arzneimittel P?tter Gmbh & Co. Kg

17 1Melissa Ag

18 1Mylan Ab

19 1NeoFarma Pharmaceuticals Limited

20 2Nico Brand Ltd

21 3Orifarm Ab

22 2Paranova Pharmaceuticals Ab

23 1Salmon Pharma Gmbh

24 1Stada Pharmaceuticals Ag

25 4Teva Bv

26 1Teva Pharma Ag

27 1Unimedic Pharma Ab

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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 :

Registration Country : Italy

Oxybutynin

Brand Name : Ditropan

Dosage Form :

Dosage Strength : 30 Cpr 5 Mg  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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 : Deregistered

Registration Country : Sweden

Oxybutynin Hydrochloride

Brand Name : Cystrin

Dosage Form : Film Coated Tablet

Dosage Strength : 5mg

Packaging :

Approval Date : 30/06/1997

Application Number : 19970630000030

Regulatory Info : Deregistered

Registration Country : Sweden

Sanofi Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : Withdrawn

Registration Country : Malta

Oxybutynin Hydrochloride

Brand Name : Ditropan

Dosage Form : Tablet

Dosage Strength : 5MG

Packaging :

Approval Date : 2006-02-28

Application Number :

Regulatory Info : Withdrawn

Registration Country : Malta

Sanofi Company Banner

04

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

Oxybutynin

Brand Name : Kentera

Dosage Form : Transdermal Patch

Dosage Strength : 3.9mg/24hours

Packaging :

Approval Date : 15/06/2004

Application Number : 20040607000526

Regulatory Info : Approved

Registration Country : Sweden

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05

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

Oxybutynin

Brand Name : Kentera

Dosage Form : Transdermal Patch

Dosage Strength : 36mg/24hours

Packaging :

Approval Date : 23/04/2007

Application Number : 57733

Regulatory Info : Allowed

Registration Country : Switzerland

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06

Neuroscience
Not Confirmed
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Neuroscience
Not Confirmed

Oxybutynin

Brand Name : Sibutinina Hydrochloride

Dosage Form : Oxybutynin Hydrochloride 5Mg 30 Joined' Oral Use

Dosage Strength : 30 CPR 5 mg

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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07

EG SpA

Country
Neuroscience
Not Confirmed
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EG SpA

Country
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Neuroscience
Not Confirmed

Oxybutynin

Brand Name : Oxybutynin

Dosage Form : Oxybutynin Hydrochloride 5Mg 30 Joined' Oral Use

Dosage Strength : 30 CPR 5 mg

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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08

Nico Brand Ltd

Country
Neuroscience
Not Confirmed
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Nico Brand Ltd

Country
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Neuroscience
Not Confirmed

Oxybutynin

Brand Name : Kentera

Dosage Form : Transdermal patches

Dosage Strength : 3.9 mg/24 hours

Packaging : Calendar Gasket

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Norway

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09

Nico Brand Ltd

Country
Neuroscience
Not Confirmed
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Nico Brand Ltd

Country
arrow
Neuroscience
Not Confirmed

Oxybutynin

Brand Name : Kentera

Dosage Form : Transdermal patches

Dosage Strength : 3.9 mg/24 hours

Packaging : Calendar Gasket

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Norway

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10

Melissa Ag

Country
Neuroscience
Not Confirmed
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Melissa Ag

Country
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Neuroscience
Not Confirmed

Oxybutynin

Brand Name : Vesoxx

Dosage Form : Solution For Injection

Dosage Strength : 1mg/ml

Packaging :

Approval Date : 27/05/2021

Application Number : 67983

Regulatory Info : Allowed

Registration Country : Switzerland

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