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
01 8Antic-calc Tablet, Film Coated
02 2FCT
03 3FILM COATED PILL
04 3FILMDRAGERAD TABLETT
05 3Film Coated Tablet
06 3Film Coated Tablet
07 4Film-Coated Tablets
08 4IR TABLET
09 1IR Tablet
10 1MUNSÖNDERFALLANDE TABLETT
11 1ODT
12 1ODT TABLET
13 1ORODISPERSIBLE TABLET
14 1Oral jelly
15 2Orally Disintegrating Tablet
16 1Orodispersible Tablet
17 1Smeltetablett
18 3TAB
19 9TABLET
20 5TABLET, ORALLY DISINTEGRATING;ORAL
21 27TABLET;ORAL
22 5Tablet
23 13Blank
01 8DISCN
02 6Generic
03 5Generic US CTD
04 3Originator
05 6Prescription
06 22RX
07 52Blank
01 3APO-VARDENAFIL
02 1Dispatigra
03 3JAMP-VARDENAFIL
04 5LEVITRA
05 19Levitra
06 2Levitra 20
07 1Levitra ODT 10
08 3Lexta
09 1STAXYN
10 1VARDENAFIL DOC
11 27VARDENAFIL HYDROCHLORIDE
12 1VARDENAFIL MYLAN
13 1VARDENAFIL TEVA ITALY
14 1VARFYDO 10 MG FC
15 1VARFYDO 20 MG FC
16 11Vivanza
17 21Blank
01 6Canada
02 3Czech Republic
03 1Egypt
04 13India
05 17Italy
06 9Norway
07 5South Africa
08 8Sweden
09 3U.A.E
10 32USA
11 5United Kingdom
Regulatory Info :
Registration Country : USA
Brand Name : VARDENAFIL HYDROCHLORIDE
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number : 203689
Regulatory Info :
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
Brand Name : VARDENAFIL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 2.5MG BASE
Packaging :
Approval Date : 2020-08-04
Application Number : 214031
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VARDENAFIL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2020-08-04
Application Number : 214031
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
Brand Name : VARDENAFIL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2018-10-31
Application Number : 210738
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : VARDENAFIL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2018-10-31
Application Number : 210738
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : VARDENAFIL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 20MG BASE
Packaging :
Approval Date : 2018-10-31
Application Number : 210738
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
Brand Name : VARDENAFIL HYDROCHLORIDE
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number : 204786
Regulatory Info :
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
Brand Name : VARDENAFIL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 20MG BASE
Packaging :
Approval Date : 2018-10-31
Application Number : 208960
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VARDENAFIL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 2.5MG BASE
Packaging :
Approval Date : 2018-10-31
Application Number : 209057
Regulatory Info : RX
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : RX
Registration Country : USA
Brand Name : VARDENAFIL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2018-10-31
Application Number : 209057
Regulatory Info : RX
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : RX
Registration Country : USA
Brand Name : VARDENAFIL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2018-10-31
Application Number : 209057
Regulatory Info : RX
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : RX
Registration Country : USA
Brand Name : VARDENAFIL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 20MG BASE
Packaging :
Approval Date : 2018-10-31
Application Number : 209057
Regulatory Info : RX
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
LOOKING FOR A SUPPLIER?
