01 3Aspen Pharmacare Holdings
02 12care4
03 4Adalvo
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 3LeBasi Pharmaceuticals (Pty) Ltd
13 2MSN Laboratories
14 3ORIFARM GROUP AS
15 3Pharma Dynamics
16 4Prinston
17 8STADA Arzneimittel
18 4Takeda Pharmaceutical
19 9Tecnimede
20 4Unichem Laboratories Limited
21 4Viatris
22 3Zydus Pharmaceuticals
01 5Antic-calc Tablet, Film Coated
02 9FCT
03 46Film Coated Tablet
04 1Oral Drop
05 2Oral Drops
06 1Oral Solution
07 11TAB
08 6TABLET
09 18TABLET;ORAL
10 4Tablet
11 9Tablet, film-coated
12 1Vortioxetina 10Mg 28 Combined Oral Use
13 1Vortioxetina 20Mg/Ml 15Ml Oral Use
14 1Vortioxetina 5Mg 28 Combined Oral Use
01 5Allowed
02 21Approved
03 19Authorized
04 1DISCN
05 18Generic
06 6Originator
07 6Prescription
08 3RX
09 36Blank
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 7TRINTELLIX
11 1Trintogen 10
12 1Trintogen 20
13 9VORTIOXETINE
14 5VORTIOXETINE HYDROBROMIDE
15 1Vorellix 10
16 1Vorellix 20
17 1Vorellix 5
18 4Vortioxetina Kern Pharma
19 4Vortioxetina Tecnigen
20 1Vortioxetine 10 mg Aspen
21 1Vortioxetine 10 mg Lundbeck
22 1Vortioxetine 20 mg Aspen
23 1Vortioxetine 20 mg Lundbeck
24 1Vortioxetine 5 mg Aspen
25 1Vortioxetine 5 mg Lundbeck
26 4Vortioxetine Adalvo
27 4Vortioxetine Amarox
28 4Vortioxetine Stada
29 4Vortioxetine Status
30 4Vortioxetine Viatris
31 1Voxbrint 10
32 1Voxbrint 20
33 1Voxbrint 5
34 9Blank
01 6Canada
02 4India
03 3Italy
04 14Norway
05 5Portugal
06 20South Africa
07 19Spain
08 21Sweden
09 5Switzerland
10 18USA
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
