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List of All Manufacturers & Suppliers of Vardenafil Hydrochloride Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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01 1Actavis Inc

02 9Alembic Pharmaceuticals Limited

03 3Apotex Inc

04 30Bayer AG

05 4CROSSMEDIKA SA

06 2Centurion Laboratories

07 1DOC Generici

08 2Farm Agon

09 7GSK

10 1Global Napi Pharmaceuticals

11 3Intas Pharmaceuticals

12 3JAMP PHARMA

13 3Jerome Stevens Pharmaceuticals

14 12Macleods Pharmaceuticals Limited

15 3Neopharma

16 1Par Pharmaceutical

17 5Teva Pharmaceutical Industries

18 1Viatris

19 4West-Coast Pharmaceuticals

20 3Zentiva

21 4Zydus Pharmaceuticals

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VARDENAFIL HYDROCHLORIDE

Brand Name : VARDENAFIL HYDROCHLORIDE

Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date :

Application Number : 203689

Regulatory Info :

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : VARDENAFIL HYDROCHLORIDE

Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2018-11-16

Application Number : 208324

Regulatory Info : RX

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : LEVITRA

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2003-08-19

Application Number : 21400

Regulatory Info : DISCN

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : LEVITRA

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2003-08-19

Application Number : 21400

Regulatory Info : DISCN

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : LEVITRA

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2003-08-19

Application Number : 21400

Regulatory Info : DISCN

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : LEVITRA

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2003-08-19

Application Number : 21400

Regulatory Info : DISCN

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : STAXYN

Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL

Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2010-06-17

Application Number : 200179

Regulatory Info : DISCN

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : VARDENAFIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2.5MG BASE

Packaging :

Approval Date : 2019-10-22

Application Number : 204632

Regulatory Info : RX

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : VARDENAFIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2019-10-22

Application Number : 204632

Regulatory Info : RX

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : VARDENAFIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2019-10-22

Application Number : 204632

Regulatory Info : RX

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : VARDENAFIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 20MG BASE

Packaging :

Approval Date : 2019-10-22

Application Number : 204632

Regulatory Info : RX

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : VARDENAFIL HYDROCHLORIDE

Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2020-03-10

Application Number : 205988

Regulatory Info : RX

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : VARDENAFIL HYDROCHLORIDE

Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date :

Application Number : 204786

Regulatory Info :

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : VARDENAFIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2.5MG BASE

Packaging :

Approval Date : 2012-05-03

Application Number : 91347

Regulatory Info : RX

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : VARDENAFIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2012-05-03

Application Number : 91347

Regulatory Info : RX

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : VARDENAFIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2012-05-03

Application Number : 91347

Regulatory Info : RX

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : VARDENAFIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 20MG BASE

Packaging :

Approval Date : 2012-05-03

Application Number : 91347

Regulatory Info : RX

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : VARDENAFIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2.5MG BASE

Packaging :

Approval Date : 2018-10-31

Application Number : 208960

Regulatory Info : RX

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : VARDENAFIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2018-10-31

Application Number : 208960

Regulatory Info : RX

Registration Country : USA

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VARDENAFIL HYDROCHLORIDE

Brand Name : VARDENAFIL HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2018-10-31

Application Number : 208960

Regulatory Info : RX

Registration Country : USA

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