01 3Aspen Pharmacare Holdings
02 12care4
03 2Adcock Ingram
04 4Alkem Laboratories
05 3Apotex Inc
06 1Cipla
07 3Cipla Medpro South Africa
08 4Farmaprojects S.A.U
09 35H. Lundbeck AS
10 3LeBasi Pharmaceuticals (Pty) Ltd
11 2MSN Laboratories
12 3ORIFARM GROUP AS
13 3Pharma Dynamics
14 4Prinston
15 4Takeda Pharmaceutical
16 5Tecnimede
17 4Unichem Laboratories Limited
18 3Zydus Pharmaceuticals
01 5Antic-calc Tablet, Film Coated
02 9FCT
03 4FILM COATED PILL
04 8Film Coated Tablet
05 1Filmtabl
06 6Filmtable
07 1ORAL DROPS, SOLUTION
08 1Oral Solution
09 11TAB
10 6TABLET
11 18TABLET;ORAL
12 4Tablet
13 9Tablet, film-coated
14 1Tropfen
15 1Vortioxetina 10Mg 28 Combined Oral Use
16 1Vortioxetina 20Mg/Ml 15Ml Oral Use
17 1Vortioxetina 5Mg 28 Combined Oral Use
01 1DISCN
02 18Generic
03 6Originator
04 3RX
05 59Blank
01 3APO-VORTIOXETINE
02 30Brintellix
03 1Brintellix 10 mg
04 1Brintellix 20 mg
05 1Brintellix 5 mg
06 1Brivor 10 mg
07 1Brivor 20 mg
08 1Brivor 5 mg
09 7TRINTELLIX
10 1Trintogen 10
11 1Trintogen 20
12 9VORTIOXETINE
13 5VORTIOXETINE HYDROBROMIDE
14 1Vorellix 10
15 1Vorellix 20
16 1Vorellix 5
17 1Vortioxetine 10 mg Aspen
18 1Vortioxetine 10 mg Lundbeck
19 1Vortioxetine 20 mg Aspen
20 1Vortioxetine 20 mg Lundbeck
21 1Vortioxetine 5 mg Aspen
22 1Vortioxetine 5 mg Lundbeck
23 1Voxbrint 10
24 1Voxbrint 20
25 1Voxbrint 5
26 13Blank
01 6Canada
02 4India
03 3Italy
04 14Norway
05 5Portugal
06 20South Africa
07 4Spain
08 5Sweden
09 8Switzerland
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
