01 3Aspen Pharmacare Holdings
02 12care4
03 4Alkem Laboratories
04 1Cipla
05 3Cipla Medpro South Africa
06 4Farmaprojects S.A.U
07 35H. Lundbeck AS
08 2MSN Laboratories
09 3ORIFARM GROUP AS
10 3Pharma Dynamics
11 4Prinston
12 4Takeda Pharmaceutical
13 5Tecnimede
14 4Unichem Laboratories Limited
15 3Zydus Pharmaceuticals
01 5Antic-calc Tablet, Film Coated
02 6FCT
03 4FILM COATED PILL
04 8Film Coated Tablet
05 1Filmtabl
06 6Filmtable
07 1ORAL DROPS, SOLUTION
08 1Oral Solution
09 9TAB
10 3TABLET
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 4DISCN
02 13Generic
03 6Originator
04 3Prescription
05 3RX
06 50Blank
01 30Brintellix
02 1Brintellix 10 mg
03 1Brintellix 20 mg
04 1Brintellix 5 mg
05 1Brivor 10 mg
06 1Brivor 20 mg
07 1Brivor 5 mg
08 7TRINTELLIX
09 9VORTIOXETINE
10 5VORTIOXETINE HYDROBROMIDE
11 1Vorellix 10
12 1Vorellix 20
13 1Vorellix 5
14 1Vortioxetine 10 mg Aspen
15 1Vortioxetine 10 mg Lundbeck
16 1Vortioxetine 20 mg Aspen
17 1Vortioxetine 20 mg Lundbeck
18 1Vortioxetine 5 mg Aspen
19 1Vortioxetine 5 mg Lundbeck
20 13Blank
01 3Canada
02 4India
03 3Italy
04 14Norway
05 5Portugal
06 15South 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 : Sweden
vortioxetinhydrobromid, anhydrous
Brand Name : Brintellix
Dosage Form : FILM COATED PILL
Dosage Strength : 15MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
vortioxetinhydrobromid, anhydrous
Brand Name : Brintellix
Dosage Form : FILM COATED PILL
Dosage Strength : 20 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Brintellix
Dosage Form : ORAL DROPS, SOLUTION
Dosage Strength : 20 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
vortioxetinhydrobromid, anhydrous
Brand Name : Brintellix
Dosage Form : FILM COATED PILL
Dosage Strength : 10 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
vortioxetinhydrobromid, anhydrous
Brand Name : Brintellix
Dosage Form : FILM COATED PILL
Dosage Strength : 5 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
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 : Generic
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : Generic
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : Generic
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 15MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : Generic
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : DISCN
Registration Country : USA
Brand Name : VORTIOXETINE HYDROBROMIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2021-09-17
Application Number : 211146
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : VORTIOXETINE HYDROBROMIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2021-09-17
Application Number : 211146
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : VORTIOXETINE HYDROBROMIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 20MG BASE
Packaging :
Approval Date : 2021-09-17
Application Number : 211146
Regulatory Info : DISCN
Registration Country : USA
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