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01 3Orion Corporation

02 1Pharmathen S.A.

03 21A Pharma A/S

04 22Care4 Aps

05 2Abacus Medicine A/S

06 3Actavis Group Ptc Ehf.

07 2Almus Farmaceutica Sau

08 1Alternova A/S

09 4Aristo Pharma Gmbh

10 1Arrow Generics Ltd

11 2Aurovitas Spain, Sau

12 3Bluefish Pharmaceuticals Ab

13 1Bmm Pharma Ab

14 1Cc Pharma Nordic Aps

15 1Combix Laboratories Slu

16 1Cross Pharma Ab

17 3Docpharma Nv

18 3Ebb Medical Ab

19 4GlaxoSmithKline AS

20 3Glaxosmithkline Ab

21 2Hexal A/S

22 1Kern Pharma Sl

23 4Medartuum Ab

24 1Orifarm A/S

25 8Orifarm Ab

26 1Orifarm Generics A/S

27 4Paranova Pharmaceuticals Ab

28 10Sandoz A/S

29 2Serra Pamies Sa Laboratories

30 1Stada Pharmaceuticals Ag

31 2Tecnimede Spain Pharmaceutical Industry Sa

32 1Teva Bv

33 3Teva Sweden Ab

34 2Viatris Limited

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PharmaCompass

01

Valaciclovir (Valacyclovir) Hydrochloride Hydrate

Brand Name : Valaciclovir Orion

Dosage Form : Film Coated Tablet

Dosage Strength : 500mg

Packaging :

Approval Date : 03/09/2010

Application Number : 20081016000028

Regulatory Info : Approved

Registration Country : Sweden

Fermion Orion Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.

Regulatory Info : Approved

Registration Country : Sweden

Valaciclovir (Valacyclovir) Hydrochloride Hydrate

Brand Name : Valaciclovir Pharmathen

Dosage Form : Film Coated Tablet

Dosage Strength : 500mg

Packaging :

Approval Date : 18/02/2011

Application Number : 20091229000029

Regulatory Info : Approved

Registration Country : Sweden

Pharmathen

03

Valaciclovir (Valacyclovir) Hydrochloride Hydrate

Brand Name : Valaciclovir Orion

Dosage Form : Film Coated Tablet

Dosage Strength : 1000mg

Packaging :

Approval Date : 03/09/2010

Application Number : 20081016000035

Regulatory Info : Deregistered

Registration Country : Sweden

Fermion Orion Company Banner

04

Valaciclovir Hydrochloride

Brand Name : Valaciclovir \"Orion\"

Dosage Form : Film Coated Tablet

Dosage Strength : 500mg

Packaging :

Approval Date : 30-06-2010

Application Number : 28104408308

Regulatory Info : Prescription

Registration Country : Denmark

Fermion Orion Company Banner

05

SCOPE Summit
Not Confirmed
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Valaciclovir (Valacyclovir) Hydrochloride Monohydrate

Brand Name : Valaciclovir Bluefish

Dosage Form : Film Coated Tablet

Dosage Strength : 500mg

Packaging :

Approval Date : 28/08/2009

Application Number : 20080308000012

Regulatory Info : Approved

Registration Country : Sweden

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06

SCOPE Summit
Not Confirmed
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SCOPE Summit
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Valaciclovir (Valacyclovir) Hydrochloride Monohydrate

Brand Name : Valaciclovir Actavis

Dosage Form : Film Coated Tablet

Dosage Strength : 500mg

Packaging :

Approval Date : 27/11/2009

Application Number : 20070801000022

Regulatory Info : Approved

Registration Country : Sweden

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07

SCOPE Summit
Not Confirmed
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SCOPE Summit
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Valaciclovir (Valacyclovir) Hydrochloride Monohydrate

Brand Name : Valaciclovir Actavis

Dosage Form : Film Coated Tablet

Dosage Strength : 1000mg

Packaging :

Approval Date : 27/11/2009

Application Number : 20070801000039

Regulatory Info : Deregistered

Registration Country : Sweden

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08

SCOPE Summit
Not Confirmed
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SCOPE Summit
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Valaciclovir (Valacyclovir) Hydrochloride Monohydrate

Brand Name : Valaciclovir Actavis

Dosage Form : Film Coated Tablet

Dosage Strength : 250mg

Packaging :

Approval Date : 27/11/2009

Application Number : 20070801000015

Regulatory Info : Deregistered

Registration Country : Sweden

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09

SCOPE Summit
Not Confirmed
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SCOPE Summit
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Valaciclovir (Valacyclovir) Hydrochloride Monohydrate

Brand Name : Valaciclovir Docpharma

Dosage Form : Film Coated Tablet

Dosage Strength : 1g

Packaging :

Approval Date : 19/04/2012

Application Number : 20070830000048

Regulatory Info : Deregistered

Registration Country : Sweden

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10

Arrow Generics Ltd

Country
SCOPE Summit
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Arrow Generics Ltd

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SCOPE Summit
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Valaciclovir (Valacyclovir) Hydrochloride Monohydrate

Brand Name : Valaciclovir Arrow

Dosage Form : Film Coated Tablet

Dosage Strength : 500mg

Packaging :

Approval Date : 27/08/2010

Application Number : 20081031000041

Regulatory Info : Deregistered

Registration Country : Sweden

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