01 12care4
02 4Alkem Laboratories
03 1Cipla
04 4Farmaprojects S.A.U
05 35H. Lundbeck AS
06 2MSN Laboratories
07 3ORIFARM GROUP AS
08 4Prinston
09 4Takeda Pharmaceutical
10 5Tecnimede
11 4Unichem Laboratories Limited
12 3Zydus Pharmaceuticals
01 5Antic-calc Tablet, Film Coated
02 4FILM COATED PILL
03 8Film Coated Tablet
04 1Filmtabl
05 6Filmtable
06 1ORAL DROPS, SOLUTION
07 1Oral Solution
08 6TAB
09 3TABLET
10 18TABLET;ORAL
11 4Tablet
12 9Tablet, film-coated
13 1Tropfen
14 1Vortioxetina 10Mg 28 Combined Oral Use
15 1Vortioxetina 20Mg/Ml 15Ml Oral Use
16 1Vortioxetina 5Mg 28 Combined Oral Use
01 1DISCN
02 4Generic
03 6Originator
04 3RX
05 56Blank
01 30Brintellix
02 1Brintellix 10 mg
03 1Brintellix 20 mg
04 1Brintellix 5 mg
05 7TRINTELLIX
06 9VORTIOXETINE
07 5VORTIOXETINE HYDROBROMIDE
08 1Vortioxetine 10 mg Lundbeck
09 1Vortioxetine 20 mg Lundbeck
10 1Vortioxetine 5 mg Lundbeck
11 13Blank
01 3Canada
02 4India
03 3Italy
04 14Norway
05 5Portugal
06 6South Africa
07 4Spain
08 5Sweden
09 8Switzerland
10 18USA
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 : Italy
Brand Name : Brintellix
Dosage Form : Vortioxetina 5Mg 28 Combined Oral Use
Dosage Strength : 28 cpr riv 5 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Brintellix
Dosage Form : Vortioxetina 10Mg 28 Combined Oral Use
Dosage Strength : 28 cpr riv 10 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Brintellix
Dosage Form : Vortioxetina 20Mg/Ml 15Ml Oral Use
Dosage Strength : os gtt 15 ml 20 mg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
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 :
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
Regulatory Info :
Registration Country : USA
Brand Name : VORTIOXETINE HYDROBROMIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 20MG BASE
Packaging :
Approval Date :
Application Number : 211146
Regulatory Info :
Registration Country : USA
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