01 2APRACLONIDINE (APRACLONIDINE HYDROCHLORIDE)
02 1Aloperidolo
03 4Apraclonidine
04 3Apraclonidine Hydrochloride
05 2Apraclonidine hydrochloride
06 1Baklofen
07 1Calcitonin, Salmon
08 1Calcitonin, Salmon, Synthetic
09 4Carbamazepine
10 1Clomipramine Hydrochloride
11 3Colistimethate Sodium
12 1Colistimethate sodium
13 1Colistin
14 2Ethosuximide
15 9Galantamine Hydrobromide
16 4Galantaminhydrobromid
17 3Gallantry
18 14Haloperidol
19 2Haloperidol Decanoate
20 1Haloperidol decanoate
21 1Lithium
22 4Methylergometrine Maleate
23 1Methylergometrinum
24 1Salmon calcitonin
01 1ESSENTIAL PHARMA LTD
02 2ESSENTIAL PHARMA SWITZERLAND GMBH
03 4Essential Pharma (M) Limited
04 5Essential Pharma (M) Ltd
05 22Essential Pharma Limited
06 16Essential Pharma Ltd
07 3Essential Pharma Ltd (Malta)
08 14Essential Pharma Switzerland Gmbh
01 7Capsule
02 2Capsule For Inhalation
03 2Coated Tablet
04 1Extended Release Capsule
05 2Extended-Release Hard Capsule
06 4Eye Drop
07 3Eye Drop Solution
08 2Eye Drops
09 1Inhalation Powder Hard Capsule
10 7Injectable Solution
11 1Oral Drops
12 1Oral Drops, Solution
13 6Oral Solution
14 2Powder For Inhalation Hard Capsule
15 2SOLUTION
16 8Solution For Injection
17 2Solution For Injection/Infusion
18 4Suppository
19 4Sustained Release Capsule
20 6Tablet
01 10.005
02 10.01
03 10.125MG
04 10.125mg
05 10.200mg/ml
06 10.2MG
07 10.2mg/ml
08 10.5%/W/V
09 11% w/v
10 11%/W/V
11 1100IU/ML
12 2100IU/ml
13 1100MG/ML
14 3100mg/ml
15 110MG
16 110mg
17 110mg/ml
18 112.5mg/ml
19 2125mg
20 41662500IU
21 116MG
22 416mg
23 31mg
24 11mg/ml
25 12 mg/ml
26 124MG
27 324mg
28 2250mg
29 22mg/ml
30 1400mg
31 14MG
32 14mg/ml
33 150MG
34 150MG/ML
35 350mg/ml
36 15MG
37 15MG/ML
38 55mg/ml
39 38mg
40 18mg, 16mg
41 3Blank
01 2Canada
02 1Estonia
03 1Italy
04 4Malta
05 14Norway
06 11Spain
07 20Sweden
08 14Switzerland
Regulatory Info :
Registration Country : Italy
Dosage Form : Oral Drops, Solution
Brand Name : HALDOL
Dosage Strength : 2 mg/ml
Packaging : 30 ML 2 MG/ML - USO ORALE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Eye Drop
Brand Name : Iopidine
Dosage Strength : 0.005
Packaging :
Approval Date : 23/03/1995
Application Number : 52813
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Eye Drop
Brand Name : Iopidine
Dosage Strength : 0.01
Packaging :
Approval Date : 26/06/1997
Application Number : 53737
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Eye Drop Solution
Brand Name : Iopidine
Dosage Strength : 5MG/ML
Packaging :
Approval Date : 2018-09-26
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Eye Drop Solution
Brand Name : Iopimax
Dosage Strength : 10MG
Packaging :
Approval Date : 01-07-1997
Application Number : 61225
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Prescription
Registration Country : Canada
APRACLONIDINE (APRACLONIDINE HYDROCHLORIDE)
Dosage Form : SOLUTION
Brand Name : IOPIDINE
Dosage Strength : 1%/W/V
Packaging :
Approval Date :
Application Number : 888354
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
APRACLONIDINE (APRACLONIDINE HYDROCHLORIDE)
Dosage Form : SOLUTION
Brand Name : IOPIDINE
Dosage Strength : 0.5%/W/V
Packaging :
Approval Date :
Application Number : 2076306
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Eye Drop
Brand Name : Iopidine
Dosage Strength : 10mg/ml
Packaging :
Approval Date : 26/04/1991
Application Number : 19910426000028
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Eye Drop
Brand Name : Iopidine
Dosage Strength : 5mg/ml
Packaging :
Approval Date : 19/12/1994
Application Number : 19941219000154
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Not Marketed
Registration Country : Norway
Dosage Form : Eye Drops
Brand Name : Iopidine
Dosage Strength : 1% w/v
Packaging :
Approval Date :
Application Number :
Regulatory Info : Not Marketed
Registration Country : Norway
