01 1Actavis Inc
02 9Alembic Pharmaceuticals Limited
03 3Apotex Inc
04 33Bayer AG
05 4CROSSMEDIKA SA
06 2Centurion Laboratories
07 1DOC Generici
08 2Farm Agon
09 7GSK
10 1Global Napi Pharmaceuticals
11 3Intas Pharmaceuticals
12 4JAMP PHARMA
13 3Jerome Stevens Pharmaceuticals
14 12Macleods Pharmaceuticals Limited
15 3Neopharma
16 1Par Pharmaceutical
17 2SANIS HEALTH INC
18 5Teva Pharmaceutical Industries
19 4Viatris
20 4West-Coast Pharmaceuticals
21 3Zentiva
22 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 6TAB
19 14TABLET
20 1TABLET (ORALLY DISINTEGRATING)
21 5TABLET, ORALLY DISINTEGRATING;ORAL
22 27TABLET;ORAL
23 5Tablet
24 13Blank
01 8DISCN
02 6Generic
03 5Generic US CTD
04 6Originator
05 12Prescription
06 22RX
07 52Blank
01 3APO-VARDENAFIL
02 1Dispatigra
03 3JAMP-VARDENAFIL
04 1JAMP-VARDENAFIL ODT
05 5LEVITRA
06 19Levitra
07 1Levitra 5
08 2Levitra 10
09 2Levitra 20
10 1Levitra ODT 10
11 3Lexta
12 3MYLAN-VARDENAFIL
13 1STAXYN
14 2VARDENAFIL
15 1VARDENAFIL DOC
16 27VARDENAFIL HYDROCHLORIDE
17 1VARDENAFIL MYLAN
18 1VARDENAFIL TEVA ITALY
19 1VARFYDO 10 MG FC
20 1VARFYDO 20 MG FC
21 11Vivanza
22 21Blank
01 12Canada
02 3Czech Republic
03 1Egypt
04 13India
05 17Italy
06 9Norway
07 8South 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 : 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Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 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
