01 1Betaxolol
02 6Betaxolol Hydrochloride
03 3Betaxolol hydrochloride
04 1Carteolol Hydrochloride
05 2Emedastin Fumarate
06 1Emedastina Difumarato
07 5Emedastindifumarat
08 2Emedastine
09 1Fluorometholone
10 1Fluorometholone Acetate
11 2Ganaxolon
12 1Ganaxolone
13 2Glycerol Phenylbutyrate
14 1Glycerol phenylbutyrate
15 1Glyceryl Phenylbutyrate
16 1Glyserolphenyl butyrate
17 1Neomycin Sulfate; Prednisone
18 4Pegzilarginase
19 6Sodium Phenylbutyrate
20 4Sodium phenylbutyrate
21 1Timolol
01 5Immedica Pharma AB
02 6Immedica Pharma AB (1)
03 36Immedica Pharma Ab
01 5Eye Drop
02 3Eye Drop Solution
03 4Eye Drop Suspension
04 8Eye Drops
05 2Eye Drops Suspension
06 4Granule
07 1Granules
08 1Injectable And Perfusion Solution
09 1Injection/Infusion Solution
10 1Mixture
11 1Ophthalmic Ointment
12 2Ophthalmic Solution
13 4Oral Liquid
14 3Oral Suspension
15 2Solution For Injection/Infusion
16 5Tablet
01 30.05% w/v
02 10.5MG
03 40.5mg/ml
04 11.1G
05 31.1g/ml
06 111g/ml
07 11MG
08 11MG/ML
09 12.5MG
10 12.5MG/ML
11 52.5mg/ml
12 120MG
13 125mg/ml
14 1500MG
15 2500mcg/ml
16 4500mg
17 350mg/ml
18 25MG
19 15MG/G;5MG/G
20 55mg/ml
21 1940MG
22 4940mg/g
01 8Denmark
02 8Estonia
03 2Malta
04 9Norway
05 10Spain
06 10Sweden
Regulatory Info : Prescription
Registration Country : Estonia
Dosage Form : Eye Drops
Brand Name : Betoptic S
Dosage Strength : 25mg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia
Regulatory Info : Withdrawn
Registration Country : Malta
Dosage Form : Eye Drop Suspension
Brand Name : Betoptic S
Dosage Strength : 2.5MG/ML
Packaging :
Approval Date : 2006-01-19
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta
Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Eye Drops
Brand Name : Betoptic
Dosage Strength : 5mg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Eye Drops Suspension
Brand Name : Betoptic S
Dosage Strength : 2.5mg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Eye Drops Suspension
Brand Name : Betoptic S
Dosage Strength : 2.5mg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Eye Drop Suspension
Brand Name : Betoptic Suspension
Dosage Strength : 2.5MG
Packaging :
Approval Date : 01-04-1996
Application Number : 61015
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Eye Drops
Brand Name : Betoptic S
Dosage Strength : 2.5mg/ml
Packaging :
Approval Date : 08-10-1993
Application Number : 28101477991
Regulatory Info : Prescription
Registration Country : Denmark
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Eye Drop
Brand Name : Betoptic
Dosage Strength : 5mg/ml
Packaging :
Approval Date : 13-06-1986
Application Number : 1.99E+13
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Eye Drop
Brand Name : Betoptic S
Dosage Strength : 2.5mg/ml
Packaging :
Approval Date : 21-02-1992
Application Number : 1.99E+13
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Eye Drop
Brand Name : Betoptic S
Dosage Strength : 2.5mg/ml
Packaging :
Approval Date : 07-02-1996
Application Number : 2.00E+13
Regulatory Info : Deregistered
Registration Country : Sweden
