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01 1Alginic Acid Alumina; Hydrated Sodium Bicarbonate

02 2Allopurinol

03 1Alumina, Hydrated; Calcium Carbonate; Sodium Alginate; Sodium Bicarbonate

04 2Amiloride Hydrochloride Dihydrate; Hydrochlorothiazide

05 1Apricot

06 1Aprotinin, Bovint

07 1Cetirizine Dihydrochloride

08 3Desloratadine

09 3Dexibuprofen

10 1Docetaxel (Vattenfri)

11 1Doxycycline Hyclate

12 1Doxycycline Monohydrate

13 2Gimeracil; Oteracil Potassium; Tegafur

14 1Glucosamine Sulfate Potassium Chloride

15 1Loperamide Hydrochloride

16 1Loperamide Hydrochloride; Simethicone

17 25Metadonhydroklorid

18 48Methotrexate

19 8Methotrexate Disodium

20 1Misoprostol

21 2My Firstborn

22 5Naloxone Hydrochloride Dihydrate; Oxycodone Hydrochloride

23 2Paracetamol

24 2Ranitidine Hydrochloride

25 1Sodium Hyaluronate

26 1Sodium Picosulfate (Monohydrate)

27 4Tegafur; Gimeracil; Oteracyl Potassium

28 1Terbinafinhydrochloride

29 3Xylometazoline Hydrochloride

30 4Ziprasidone Hydrochloride (Anhydrous)

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PharmaCompass

01

Brand Name : Gaviscon

FNCE
Not Confirmed
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Brand Name : Gaviscon

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FNCE
Not Confirmed

Nordic Drugs

Dosage Form : Chewable Tablet

Dosage Strength :

Packaging :

Brand Name : Gaviscon

Approval Date : 30/08/1974

Application Number : 19740830000013

Regulatory Info : Approved

Registration Country : Sweden

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02

Brand Name : Allopurinol Nordic D...

FNCE
Not Confirmed
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Brand Name : Allopurinol Nordic D...

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FNCE
Not Confirmed

Nordic Drugs

Dosage Form : Tablet

Dosage Strength : 100mg

Packaging :

Brand Name : Allopurinol Nordic Drugs

Approval Date : 25/01/1991

Application Number : 19910125000015

Regulatory Info : Approved

Registration Country : Sweden

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03

Brand Name : Allopurinol Nordic D...

FNCE
Not Confirmed
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Brand Name : Allopurinol Nordic D...

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FNCE
Not Confirmed

Nordic Drugs

Dosage Form : Tablet

Dosage Strength : 300mg

Packaging :

Brand Name : Allopurinol Nordic Drugs

Approval Date : 25/01/1991

Application Number : 19910125000022

Regulatory Info : Approved

Registration Country : Sweden

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04

Brand Name : Gaviscon

FNCE
Not Confirmed
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Brand Name : Gaviscon

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FNCE
Not Confirmed

Nordic Drugs

Dosage Form : Oral Suspension

Dosage Strength :

Packaging :

Brand Name : Gaviscon

Approval Date : 05/02/1982

Application Number : 19820205000135

Regulatory Info : Approved

Registration Country : Sweden

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05

Brand Name : Amyloferm

FNCE
Not Confirmed
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Brand Name : Amyloferm

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FNCE
Not Confirmed

Nordic Drugs

Dosage Form : Tablet

Dosage Strength : 5mg;50mg

Packaging :

Brand Name : Amyloferm

Approval Date : 04/05/1990

Application Number : 19900504000149

Regulatory Info : Approved

Registration Country : Sweden

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06

Brand Name : Amyloferm Mite

FNCE
Not Confirmed
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Brand Name : Amyloferm Mite

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FNCE
Not Confirmed

Nordic Drugs

Dosage Form : Tablet

Dosage Strength : 2.5mg;25mg

Packaging :

Brand Name : Amyloferm Mite

Approval Date : 04/05/1990

Application Number : 19900504000156

Regulatory Info : Approved

Registration Country : Sweden

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07

Brand Name : Trasylol

FNCE
Not Confirmed
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Brand Name : Trasylol

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FNCE
Not Confirmed

Nordic Pharma

Dosage Form : Solution For Injection/Infusio...

Dosage Strength :

Packaging :

Brand Name : Trasylol

Approval Date : 16/03/1977

Application Number : 38837

Regulatory Info : Allowed

Registration Country : Switzerland

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08

Brand Name : Trasylol

FNCE
Not Confirmed
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Brand Name : Trasylol

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FNCE
Not Confirmed

Nordic Pharma

Dosage Form : Solution For Injection/Infusio...

Dosage Strength : 10000KIE/ml

Packaging :

Brand Name : Trasylol

Approval Date : 13/12/1967

Application Number : 19671213000033

Regulatory Info : Approved

Registration Country : Sweden

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09

Brand Name : Acura

FNCE
Not Confirmed
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Brand Name : Acura

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FNCE
Not Confirmed

Nordic Drugs

Dosage Form : Film Coated Tablet

Dosage Strength : 10mg

Packaging :

Brand Name : Acura

Approval Date : 19/04/2002

Application Number : 20020419000112

Regulatory Info : Deregistered

Registration Country : Sweden

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10

Brand Name : Desloraphar

FNCE
Not Confirmed
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Brand Name : Desloraphar

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FNCE
Not Confirmed

Disphar International

Dosage Form : Film Coated Tablet

Dosage Strength : 5mg

Packaging :

Brand Name : Desloraphar

Approval Date : 13/09/2012

Application Number : 20110121000033

Regulatory Info : Deregistered

Registration Country : Sweden

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