01 3Aspen Pharmacare Holdings
02 12care4
03 8Adalvo
04 2Adcock Ingram
05 4Alkem Laboratories
06 4Amarox Pharma Bv
07 3Apotex Inc
08 1Cipla
09 3Cipla Medpro South Africa
10 39H. Lundbeck AS
11 4Kern Pharma S.L.
12 6LeBasi Pharmaceuticals CC
13 2MSN Laboratories
14 4Macleods Pharmaceuticals Limited
15 3ORIFARM GROUP AS
16 3Pharma Dynamics
17 4Prinston
18 8STADA Arzneimittel
19 4Takeda Pharmaceutical
20 9Tecnimede
21 4Unichem Laboratories Limited
22 4Viatris
23 3Zydus Pharmaceuticals
01 5Antic-calc Tablet, Film Coated
02 12FCT
03 50Film Coated Tablet
04 1Oral Drop
05 2Oral Drops
06 1Oral Solution
07 11TAB
08 6TABLET
09 4TABLET:FILM COATED
10 18TABLET;ORAL
11 4Tablet
12 9Tablet, film-coated
13 1Vortioxetina 10Mg 28 Combined Oral Use
14 1Vortioxetina 20Mg/Ml 15Ml Oral Use
15 1Vortioxetina 5Mg 28 Combined Oral Use
01 5Allowed
02 21Approved
03 4Authorised
04 19Authorized
05 1DISCN
06 21Generic
07 6Originator
08 6Prescription
09 3RX
10 40Blank
01 3APO-VORTIOXETINE
02 30Brintellix
03 1Brintellix 10 mg
04 1Brintellix 20 mg
05 1Brintellix 5 mg
06 4Brintellix film-coated tablets
07 1Brivor 10 mg
08 1Brivor 20 mg
09 1Brivor 5 mg
10 4Jimb
11 1Netixev 10
12 1Netixev 20
13 1Netixev 5
14 7TRINTELLIX
15 1Trintogen 10
16 1Trintogen 20
17 9VORTIOXETINE
18 9VORTIOXETINE HYDROBROMIDE
19 1Vorellix 10
20 1Vorellix 20
21 1Vorellix 5
22 4Vortioxetina Kern Pharma
23 4Vortioxetina Tecnigen
24 1Vortioxetine 10 mg Aspen
25 1Vortioxetine 10 mg Lundbeck
26 1Vortioxetine 20 mg Aspen
27 1Vortioxetine 20 mg Lundbeck
28 1Vortioxetine 5 mg Aspen
29 1Vortioxetine 5 mg Lundbeck
30 4Vortioxetine Adalvo
31 4Vortioxetine Amarox
32 4Vortioxetine Stada
33 4Vortioxetine Status
34 4Vortioxetine Viatris
35 1Voxbrint 10
36 1Voxbrint 20
37 1Voxbrint 5
38 9Blank
01 6Canada
02 4India
03 3Italy
04 4Malta
05 14Norway
06 5Portugal
07 23South Africa
08 19Spain
09 21Sweden
10 5Switzerland
11 22USA
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Vortioxetine 5 mg Aspen
Dosage Form : TAB
Dosage Strength : 5mg
Packaging : 30X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Vortioxetine 10 mg Aspen
Dosage Form : TAB
Dosage Strength : 10mg
Packaging : 30X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Vortioxetine 20 mg Aspen
Dosage Form : TAB
Dosage Strength : 20mg
Packaging : 30X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info :
Registration Country : USA
Brand Name : VORTIOXETINE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number : 211089
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : VORTIOXETINE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number : 211089
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : VORTIOXETINE
Dosage Form : TABLET;ORAL
Dosage Strength : 15MG
Packaging :
Approval Date :
Application Number : 211089
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : VORTIOXETINE
Dosage Form : TABLET;ORAL
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number : 211089
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : VORTIOXETINE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number : 211085
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : VORTIOXETINE HYDROBROMIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number : 211101
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : VORTIOXETINE HYDROBROMIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number : 211101
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : VORTIOXETINE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number : 211024
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : VORTIOXETINE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number : 211024
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : VORTIOXETINE
Dosage Form : TABLET;ORAL
Dosage Strength : 15MG
Packaging :
Approval Date :
Application Number : 211024
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : VORTIOXETINE
Dosage Form : TABLET;ORAL
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number : 211024
Regulatory Info :
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TRINTELLIX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2013-09-30
Application Number : 204447
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TRINTELLIX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2013-09-30
Application Number : 204447
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TRINTELLIX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2013-09-30
Application Number : 204447
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TRINTELLIX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 20MG BASE
Packaging :
Approval Date : 2013-09-30
Application Number : 204447
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : VORTIOXETINE HYDROBROMIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date :
Application Number : 211146
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : VORTIOXETINE HYDROBROMIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date :
Application Number : 211146
Regulatory Info :
Registration Country : USA
