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01 4 Vancomycin Hydrochloride
02 4Amoxicillin Trihydrate
03 1Cefazolin
04 1Cefazolinnatrium
05 2Cefepima
06 2Cefepimdihydrokloridmonohydrat
07 2Cefepime
08 2Cefotaxime
09 2Cefotaximnatrium
10 2Ceftazidime
11 2Ceftazidime Pentahydrate
12 2Ceftriaxone Sodium
13 2Ceftriaxonnatrium (Hemiheptahydrat)
14 4Cefuroxime Sodium
15 1Citronsyra (Vattenfri) Kaliumklorid Makrogol Natriumcitrat (Dihydrat) Natriumklorid
16 2Daptomycin
17 2Glucosamine Sulfate Magnesium Chloride (2:1:1:2)
18 2Laktulos
19 2Macrogol 4000
20 2Vancomycin
21 2Vancomycin Hydrochloride
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01 1Concentrate For Oral Solution
02 2Concentrate to potion, resolution
03 2Film Coated Tablet
04 9Injection/Infusion Solution
05 1Oral Gel
06 1Oral Solution
07 4Powder For Injection And Infusion Solution
08 1Powder For Oral Suspension
09 2Powder For Solution For Infusion
10 1Powder For Solution For Injection
11 3Powder for infusion fluid, resolution
12 1Powder for injection fluid, resolution
13 9Powder for injection/infusion fluid, resolution
14 5Solution For Injection
15 3Tablet
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01 2(not entered)
02 51 g
03 11.5 g
04 11000MG
05 31000mg
06 11500mg
07 21G
08 31g
09 52 g
10 22G
11 1350mg
12 2400mg
13 1500 mg
14 1500MG
15 4500mg
16 150mg/ml
17 2650mg/ml
18 1750 mg
19 2750mg
20 5Blank
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01 15Norway
02 6Spain
03 24Sweden
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01 4Amoxicillin Mip
02 1Cefazolin MIP
03 1Cefazolin Mip
04 2Cefepim MIP
05 2Cefepim Mip
06 2Cefepima Mip
07 2Cefotaxim MIP
08 2Cefotaxim Mip
09 2Ceftazidim MIP
10 2Ceftazidime Mip
11 2Ceftriaxon MIP
12 2Ceftriaxon Mip
13 2Cefuroxim MIP
14 2Cefuroxim Mip
15 2Daptomycin Mip
16 1Glukosamin Mip
17 1Lactulade
18 1Laktulos Mip
19 3Olopeg
20 1Perigona
21 2Vancomicina Mip
22 2Vancomycin MIP
23 2Vancomycin Mip
24 2Vancosan
Regulatory Info :
Registration Country : Norway
Dosage Form : Powder for injection/infusion ...
Dosage Strength : 2 g
Packaging : Hood glass
Brand Name : Cefazolin MIP
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Tablet
Dosage Strength : 1000mg
Packaging :
Brand Name : Amoxicillin Mip
Approval Date : 19/04/2012
Application Number : 20100326000051
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Powder For Oral Suspension
Dosage Strength : 50mg/ml
Packaging :
Brand Name : Amoxicillin Mip
Approval Date : 19/04/2012
Application Number : 20100330000016
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Tablet
Dosage Strength : 500mg
Packaging :
Brand Name : Amoxicillin Mip
Approval Date : 19/04/2012
Application Number : 20100326000037
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Tablet
Dosage Strength : 750mg
Packaging :
Brand Name : Amoxicillin Mip
Approval Date : 19/04/2012
Application Number : 20100326000044
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Injection/Infusion Solution
Dosage Strength :
Packaging :
Brand Name : Cefazolin Mip
Approval Date : 20/03/2014
Application Number : 20111130000014
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Solution For Injection
Dosage Strength : 1000mg
Packaging :
Brand Name : Vancomycin Mip
Approval Date : 07/10/2005
Application Number : 20040607009246
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Solution For Injection
Dosage Strength : 500mg
Packaging :
Brand Name : Vancomycin Mip
Approval Date : 07/10/2005
Application Number : 20040607009239
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Solution For Injection
Dosage Strength : 1000mg
Packaging :
Brand Name : Vancosan
Approval Date : 08/07/2011
Application Number : 20100227000051
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Solution For Injection
Dosage Strength : 500mg
Packaging :
Brand Name : Vancosan
Approval Date : 08/07/2011
Application Number : 20100227000044
Regulatory Info : Deregistered
Registration Country : Sweden