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01 2Intas Pharmaceuticals
02 2MSN Laboratories
03 2Natco Pharma
04 10Servier
05 2Servier Laboratories S.A. (Pty) Ltd
06 4Taiho Pharmaceutical
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01 1FCT
02 10Film Coated Tablet
03 1TAB
04 2TABLET
05 6TABLET;ORAL
06 2Tablet
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01 2Allowed
02 2Approved
03 6Authorized
04 2Originator
05 2Prescription
06 6RX
07 2Blank
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01 4LONSURF
02 1LONSURF15 mg/6,14 mg
03 1LONSURF20 mg/8.19 mg
04 8Lonsurf
05 2Lonsurf
06 4TIPIRACIL HYDROCHLORIDE AND TRIFLURIDINE
07 2Blank
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01 2Canada
02 2India
03 2South Africa
04 6Spain
05 2Sweden
06 2Switzerland
07 6USA
Regulatory Info :
Registration Country : India
Tipiracil Hydrochloride; Trifluridine
Brand Name :
Dosage Form : Tablet
Dosage Strength : 15MG; 6.14MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Tipiracil Hydrochloride; Trifluridine
Brand Name :
Dosage Form : Tablet
Dosage Strength : 20MG; 8.19MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : RX
Registration Country : USA
TIPIRACIL HYDROCHLORIDE; TRIFLURIDINE
Brand Name : TIPIRACIL HYDROCHLORIDE AND TRIFLURIDINE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 6.14MG BASE;15MG
Packaging :
Approval Date : 2025-01-08
Application Number : 214024
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
TIPIRACIL HYDROCHLORIDE; TRIFLURIDINE
Brand Name : TIPIRACIL HYDROCHLORIDE AND TRIFLURIDINE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 8.19MG BASE;20MG
Packaging :
Approval Date : 2025-01-08
Application Number : 214024
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
TIPIRACIL HYDROCHLORIDE; TRIFLURIDINE
Brand Name : TIPIRACIL HYDROCHLORIDE AND TRIFLURIDINE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 6.14MG BASE;15MG
Packaging :
Approval Date : 2023-06-13
Application Number : 214008
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
TIPIRACIL HYDROCHLORIDE; TRIFLURIDINE
Brand Name : TIPIRACIL HYDROCHLORIDE AND TRIFLURIDINE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 8.19MG BASE;20MG
Packaging :
Approval Date : 2023-06-13
Application Number : 214008
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Approved
Registration Country : Sweden
Tipiracil Hydrochloride; Trifluridine
Brand Name : Lonsurf
Dosage Form : Film Coated Tablet
Dosage Strength : 15mg;6.14mg
Packaging :
Approval Date : 25/04/2016
Application Number : 20150401000018
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Tipiracil Hydrochloride; Trifluridine
Brand Name : Lonsurf
Dosage Form : Film Coated Tablet
Dosage Strength : 20mg;8.19mg
Packaging :
Approval Date : 25/04/2016
Application Number : 20150401000025
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Lonsurf
Dosage Form : Film Coated Tablet
Dosage Strength : 15mg;6.14mg
Packaging :
Approval Date : 25/08/2017
Application Number : 66219
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Lonsurf
Dosage Form : Film Coated Tablet
Dosage Strength : 20mg;8.19mg
Packaging :
Approval Date : 25/08/2017
Application Number : 66219
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Lonsurf
Dosage Form : Film Coated Tablet
Dosage Strength : 15MG; 6.14 MG
Packaging :
Approval Date : 2021-06-21
Application Number : 1161096001IP
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Lonsurf
Dosage Form : Film Coated Tablet
Dosage Strength : 20MG; 8.19 MG
Packaging :
Approval Date : 2016-06-01
Application Number : 1161096004
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Lonsurf
Dosage Form : Film Coated Tablet
Dosage Strength : 15MG; 6.14 MG
Packaging :
Approval Date : 2016-06-01
Application Number : 1161096003
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Lonsurf
Dosage Form : Film Coated Tablet
Dosage Strength : 20MG; 8.19 MG
Packaging :
Approval Date : 2016-06-01
Application Number : 1161096006
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : RX
Registration Country : USA
TIPIRACIL HYDROCHLORIDE; TRIFLURIDINE
Brand Name : LONSURF
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 6.14MG BASE;15MG
Packaging :
Approval Date : 2015-09-22
Application Number : 207981
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
TIPIRACIL HYDROCHLORIDE; TRIFLURIDINE
Brand Name : LONSURF
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 8.19MG BASE;20MG
Packaging :
Approval Date : 2015-09-22
Application Number : 207981
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
TIPIRACIL (TIPIRACIL HYDROCHLORIDE)
Brand Name : LONSURF
Dosage Form : TABLET
Dosage Strength : 6.14MG
Packaging : 20
Approval Date :
Application Number : 2472104
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
TIPIRACIL (TIPIRACIL HYDROCHLORIDE)
Brand Name : LONSURF
Dosage Form : TABLET
Dosage Strength : 8.19MG
Packaging : 20
Approval Date :
Application Number : 2472112
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : LONSURF20 mg/8.19 mg
Dosage Form : TAB
Dosage Strength : 8.19mg
Packaging : 20X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : LONSURF15 mg/6,14 mg
Dosage Form : FCT
Dosage Strength : 6.14mg
Packaging : 20X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF