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01 1?resund Pharma Aps
02 5Alcon Inc
03 4Alliance Pharmaceutical Company
04 1B. Braun Melsungen AG
05 1Fresenius Kabi AB Brunna
06 2Hanlim Pharmaceuticals Inc
07 1Juno Pharmaceuticals Pty Ltd
08 5Meda - Asker
09 4Meda Ab
10 2Pfizer Inc
11 2Pharmanovia A/S
12 1Reva Health
13 1TEOFARMA Srl
14 2World Medicine
15 1Xvivo Perfusion Ab
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01 2DROPS
02 2EYE DROP
03 2EYE DROPS
04 2Eye Drop
05 1INF
06 2INJ
07 5Infusion Solution
08 5Infusion fluid, resolution
09 1Injectable Solution
10 2Injection fluid, resolution
11 1SOL
12 4SOLUTION
13 2Solution
14 1Solution For Injection
15 1Blank
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01 1Allowed
02 1Approved
03 2Cancelled
04 7Deregistered
05 2Ethical
06 3Generic
07 4NON-PRESCRIPTION DRUGS
08 3Originator
09 10Blank
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01 1ADVANCED RELIEF EYE DROPS
02 1Bion Tears
03 1CLEAR-DROP
04 1Dacrolux
05 1LMD 10% IN 0.9% SODIUM CHLORIDE
06 1LMD 10% IN DEXTROSE 5%
07 1Macrodex 6% In Normal Saline
08 1Macrodex 60 Mg/Ml Med Natriumklorid
09 1Macrodex with sodium chloride
10 1NUMAREN
11 1Natural Tears
12 1Perfadex
13 2Plasmodex
14 1Promit 150Mg/Ml
15 3Promiten
16 2Rescue flow
17 2Rescueflow
18 1Rheomacrodex 10% In Normal Saline
19 1Rheomacrodex 10% Saline
20 1Rheomacrodex 100 Mg/Ml With Sodium Chloride
21 1Rheomacrodex with sodium chloride
22 1Ringer-Dextran 60
23 1SLEZOL FORTE
24 1SLEZOL-D
25 1Stranoval
26 1TEARS NATURALE FORTE
27 1TEARS NATURALE FREE
28 1TEARS NATURALE II
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01 6Canada
02 1Italy
03 7Norway
04 4South Africa
05 2South Korea
06 2Spain
07 8Sweden
08 1Switzerland
09 2Turkey
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Bion Tears
Dosage Form : Eye Drop
Dosage Strength :
Packaging :
Approval Date : 19/10/2001
Application Number : 20011019000053
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dextran 60; Calcium Chloride Dihydrate; Potassium Chloride; Magnesium Chloride Hexahydrate; Sodium Acetate Trihydrate; Sodium Chloride
Brand Name : Ringer-Dextran 60
Dosage Form : Infusion Solution
Dosage Strength :
Packaging :
Approval Date : 28/08/1992
Application Number : 19920828000021
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Generic
Registration Country : South Korea
Brand Name : NUMAREN
Dosage Form : EYE DROP
Dosage Strength : 3MG; 1MG
Packaging : 15mL, 0.6mL,30ea
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info : Generic
Registration Country : South Korea
Tetrahydrozoline; Dextrans; N-Vinyl-2-Pyrrolidone; Polyethylene Glycol Monostearate
Brand Name : CLEAR-DROP
Dosage Form : EYE DROP
Dosage Strength : 0.5MG/ML; 2MG/ML; 10MG/ML; 10
Packaging : 15mL
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info :
Registration Country : Turkey
Brand Name : SLEZOL-D
Dosage Form : EYE DROPS
Dosage Strength : 3MG; 1MG
Packaging : 15 ML/BOTTLE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Turkey
Regulatory Info :
Registration Country : Turkey
Hypromellose API; Dextrans; Glycerine
Brand Name : SLEZOL FORTE
Dosage Form : EYE DROPS
Dosage Strength : 3MG; 1MG; 2MG
Packaging : 15 ML/BOTTLE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Turkey
Regulatory Info :
Registration Country : Italy
Brand Name : Stranoval
Dosage Form :
Dosage Strength : Cream Derm 30 G 0.122% + 32,000 I.U./100 G_
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
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Regulatory Info :
Registration Country : Norway
Brand Name : Macrodex with sodium chloride
Dosage Form : Infusion fluid, resolution
Dosage Strength : 60 mg/ml
Packaging : Plastic bag
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
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Regulatory Info :
Registration Country : Norway
Brand Name : Plasmodex
Dosage Form : Infusion fluid, resolution
Dosage Strength : 30 g/1000 ml
Packaging : Plastic bag
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
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Regulatory Info :
Registration Country : Norway
Brand Name : Promiten
Dosage Form : Injection fluid, resolution
Dosage Strength : 150 mg/ml
Packaging : Hood glass
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
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Regulatory Info :
Registration Country : Norway
Brand Name : Promiten
Dosage Form : Injection fluid, resolution
Dosage Strength : 150 mg/ml
Packaging : Ampoule of plastic
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
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Regulatory Info :
Registration Country : Norway
Brand Name : Rescue flow
Dosage Form : Infusion fluid, resolution
Dosage Strength : 60 g/l/75 g/l
Packaging : Plastic bag
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
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Regulatory Info :
Registration Country : Norway
Brand Name : Rescue flow
Dosage Form : Infusion fluid, resolution
Dosage Strength : 60 g/l/75 g/l
Packaging : Plastic bag
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
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Regulatory Info :
Registration Country : Norway
Brand Name : Rheomacrodex with sodium chloride
Dosage Form : Infusion fluid, resolution
Dosage Strength : 100 mg/ml
Packaging : Plastic bag
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
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Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Promiten
Dosage Form : Injectable Solution
Dosage Strength : 150mg/ml
Packaging :
Approval Date : 22/10/1982
Application Number : 19821022000056
Regulatory Info : Deregistered
Registration Country : Sweden
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Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Rheomacrodex 100 Mg/Ml With Sodium Chloride
Dosage Form : Infusion Solution
Dosage Strength : 100mg/ml
Packaging :
Approval Date : 15/12/1961
Application Number : 19611215000013
Regulatory Info : Deregistered
Registration Country : Sweden
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Regulatory Info : Deregistered
Registration Country : Sweden
Dextran 40; Disodium Phosphate Dodecahydrate; Glucose Monohydrate; Potassium Dihydrogen Phosphate; Potassium Chloride; Magnesium Sulfate Heptahydrate; Sodium Chloride
Brand Name : Perfadex
Dosage Form : Solution
Dosage Strength :
Packaging :
Approval Date : 22/05/1970
Application Number : 19700522000035
Regulatory Info : Deregistered
Registration Country : Sweden
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Regulatory Info : Deregistered
Registration Country : Sweden
Dextran 60; Calcium Chloride Dihydrate; Potassium Chloride; Magnesium Chloride Hexahydrate; Sodium Acetate Anhydrous; Sodium Chloride
Brand Name : Plasmodex
Dosage Form : Infusion Solution
Dosage Strength :
Packaging :
Approval Date : 08/12/1989
Application Number : 19891208000125
Regulatory Info : Deregistered
Registration Country : Sweden
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Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Macrodex 60 Mg/Ml Med Natriumklorid
Dosage Form : Infusion Solution
Dosage Strength : 60mg/ml
Packaging :
Approval Date : 28/11/1955
Application Number : 19551128000017
Regulatory Info : Deregistered
Registration Country : Sweden
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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Rescueflow
Dosage Form : Infusion Solution
Dosage Strength :
Packaging :
Approval Date : 17/11/1998
Application Number : 19981117000023
Regulatory Info : Approved
Registration Country : Sweden
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