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01 5AbbVie Inc
02 2Norvium
03 1Solvay
04 7Viatris
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01 8Film Coated Tablet
02 7TABLET;ORAL
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01 6Authorized
02 7DISCN
03 2Deregistered
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01 1Co-Operation
02 2EPROSARTAN MESYLATE
03 1Futuran Plus
04 1Future
05 1Navixen Plus
06 1Regulate
07 1Regulaten Plus
08 3TEVETEN
09 2TEVETEN HCT
10 1Teveten Comp
11 1Tevetens Plus
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01 6Spain
02 2Sweden
03 7USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TEVETEN
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1997-12-22
Application Number : 20738
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TEVETEN
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1997-12-22
Application Number : 20738
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TEVETEN
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 600MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1999-05-27
Application Number : 20738
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
EPROSARTAN MESYLATE; HYDROCHLOROTHIAZIDE
Brand Name : TEVETEN HCT
Dosage Form : TABLET;ORAL
Dosage Strength : 600MG;12.5MG
Packaging :
Approval Date : 2001-11-01
Application Number : 21268
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
EPROSARTAN MESYLATE; HYDROCHLOROTHIAZIDE
Brand Name : TEVETEN HCT
Dosage Form : TABLET;ORAL
Dosage Strength : 600MG;25MG
Packaging :
Approval Date : 2001-11-01
Application Number : 21268
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : EPROSARTAN MESYLATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 400MG BASE
Packaging :
Approval Date : 2011-11-16
Application Number : 202012
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : EPROSARTAN MESYLATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 600MG BASE
Packaging :
Approval Date : 2011-11-16
Application Number : 202012
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Deregistered
Registration Country : Sweden
Eprosartan Mesilate Hydrochlorothiazide
Brand Name : Co-Operation
Dosage Form : Film Coated Tablet
Dosage Strength : 600mg;12.5mg
Packaging :
Approval Date : 01/09/2006
Application Number : 20060112000231
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Eprosartan Mesilate Hydrochlorothiazide
Brand Name : Teveten Comp
Dosage Form : Film Coated Tablet
Dosage Strength : 600mg;12.5mg
Packaging :
Approval Date : 17/09/2004
Application Number : 20040607006108
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Authorized
Registration Country : Spain
Hydrochlorothiazide; Eprosartan Mesylate Dihydrate
Brand Name : Navixen Plus
Dosage Form : Film Coated Tablet
Dosage Strength : 600MG; 12.5 MG
Packaging :
Approval Date : 2004-12-17
Application Number : 66512
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Hydrochlorothiazide; Eprosartan Mesylate Dihydrate
Brand Name : Regulaten Plus
Dosage Form : Film Coated Tablet
Dosage Strength : 600MG; 12.5 MG
Packaging :
Approval Date : 2005-01-13
Application Number : 66528
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Hydrochlorothiazide; Eprosartan Mesylate Dihydrate
Brand Name : Tevetens Plus
Dosage Form : Film Coated Tablet
Dosage Strength : 600MG; 12.5 MG
Packaging :
Approval Date : 2004-07-01
Application Number : 66206
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Hydrochlorothiazide; Eprosartan Mesylate Dihydrate
Brand Name : Futuran Plus
Dosage Form : Film Coated Tablet
Dosage Strength : 600MG; 12.5 MG
Packaging :
Approval Date : 2005-01-28
Application Number : 66568
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Regulate
Dosage Form : Film Coated Tablet
Dosage Strength : 600MG
Packaging :
Approval Date : 2000-12-04
Application Number : 63509
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Future
Dosage Form : Film Coated Tablet
Dosage Strength : 600MG
Packaging :
Approval Date : 2002-02-22
Application Number : 64578
Regulatory Info : Authorized
Registration Country : Spain