01 3Aspen Pharmacare Holdings
02 12care4
03 1Abacus Medicine
04 8Adalvo
05 2Adcock Ingram
06 4Alkem Laboratories
07 4Amarox Pharma Bv
08 3Apotex Inc
09 3Ascend Labs
10 1Cipla
11 3Cipla Medpro South Africa
12 4Grindeks AS
13 32H. Lundbeck AS
14 4Krka
15 6LeBasi Pharmaceuticals CC
16 2MSN Laboratories
17 4Macleods Pharmaceuticals Limited
18 3ORIFARM GROUP AS
19 3Pharma Dynamics
20 4Prinston
21 4STADA Arzneimittel
22 4Takeda Pharmaceutical
23 5Tecnimede
24 4Unichem Laboratories Limited
25 4Viatris
26 3Zydus Pharmaceuticals
01 12FCT
02 42Film Coated Tablet
03 8Film-Coated Tablet
04 2Oral Drops
05 1Oral Drops Solution
06 1Oral Solution
07 14TAB
08 6TABLET
09 4TABLET:FILM COATED
10 18TABLET;ORAL
11 4Tablet
12 1Vortioxetina 10Mg 28 Combined Oral Use
13 1Vortioxetina 20Mg/Ml 15Ml Oral Use
14 1Vortioxetina 5Mg 28 Combined Oral Use
15 4Blank
01 5Allowed
02 21Approved
03 4Authorised
04 1DISCN
05 24Generic
06 10Marketed
07 6Originator
08 15Prescription
09 3RX
10 30Blank
01 3APO-VORTIOXETINE
02 24Brintellix
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 4Varesta
20 1Vorellix 10
21 1Vorellix 20
22 1Vorellix 5
23 1Vortioxetine 10 mg Aspen
24 1Vortioxetine 10 mg Lundbeck
25 1Vortioxetine 20 mg Aspen
26 1Vortioxetine 20 mg Lundbeck
27 1Vortioxetine 5 mg Aspen
28 1Vortioxetine 5 mg Lundbeck
29 4Vortioxetine Adalvo
30 4Vortioxetine Amarox
31 4Vortioxetine Stada
32 4Vortioxetine Viatris
33 1Voxbrint 10
34 1Voxbrint 20
35 1Voxbrint 5
36 1Xirov 10
37 1Xirov 20
38 1Xirov 5
39 13Blank
01 6Canada
02 9Estonia
03 4India
04 3Italy
05 4Latvia
06 4Malta
07 10Norway
08 5Portugal
09 26South Africa
10 21Sweden
11 5Switzerland
12 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
