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01 1Alcon Inc

02 1Boiron Iberian Society Of Homeopathy Sa

03 10Essential Pharma

04 2Harrow

05 2Novartis South Africa (Pty) Ltd

06 2ORIFARM GROUP AS

07 2Paranova Pharmaceuticals Ab

08 1Rising Pharmaceuticals Inc

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PharmaCompass

01

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Apraclonidine

Brand Name : Iopidine

Dosage Form : Apraclonidina 5Mg/Ml 5Ml Solution Ophthalmic Use

Dosage Strength : EYE DROPS 5 ml 5 mg/ml

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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02

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Apraclonidine

Brand Name : Iopidine

Dosage Form : Eye Drop Solution

Dosage Strength : 5MG/ML

Packaging :

Approval Date : 2018-09-26

Application Number :

Regulatory Info : Authorised

Registration Country : Malta

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03

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Apraclonidine hydrochloride

Brand Name : Iopidine

Dosage Form : Eye Drops

Dosage Strength : 1% w/v

Packaging :

Approval Date :

Application Number :

Regulatory Info : Not Marketed

Registration Country : Norway

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04

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Apraclonidine hydrochloride

Brand Name : Iopidine

Dosage Form : Eye Drops

Dosage Strength : 5mg/ml

Packaging :

Approval Date :

Application Number :

Regulatory Info : Marketed

Registration Country : Norway

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05

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Apraclonidine Hydrochloride

Brand Name : Iopimax

Dosage Form : Eye Drop Solution

Dosage Strength : 5MG

Packaging :

Approval Date : 01-10-1996

Application Number : 60634

Regulatory Info : Authorized

Registration Country : Spain

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06

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Apraclonidine Hydrochloride

Brand Name : Iopidine

Dosage Form : Eye Drops

Dosage Strength : 10mg/ml

Packaging :

Approval Date : 12-04-1996

Application Number : 28101792195

Regulatory Info : Prescription

Registration Country : Denmark

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07

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Apraclonidine Hydrochloride

Brand Name : Iopidine

Dosage Form : Eye Drops

Dosage Strength : 5mg/ml

Packaging :

Approval Date : 31-07-1995

Application Number : 28101557693

Regulatory Info : Prescription

Registration Country : Denmark

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08

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Apraclonidine Hydrochloride

Brand Name : Iopidine

Dosage Form : Eye Drop

Dosage Strength : 10mg/ml

Packaging :

Approval Date : 26-04-1991

Application Number : 1.99E+13

Regulatory Info : Approved

Registration Country : Sweden

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09

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Apraclonidine Hydrochloride

Brand Name : Iopidine

Dosage Form : Eye Drop

Dosage Strength : 5mg/ml

Packaging :

Approval Date : 19-12-1994

Application Number : 1.99E+13

Regulatory Info : Approved

Registration Country : Sweden

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10

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

APRACLONIDINE (APRACLONIDINE HYDROCHLORIDE)

Brand Name : IOPIDINE

Dosage Form : SOLUTION

Dosage Strength : 1%/W/V

Packaging :

Approval Date :

Application Number : 888354

Regulatory Info : Prescription

Registration Country : Canada

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11

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

APRACLONIDINE (APRACLONIDINE HYDROCHLORIDE)

Brand Name : IOPIDINE

Dosage Form : SOLUTION

Dosage Strength : 0.5%/W/V

Packaging :

Approval Date :

Application Number : 2076306

Regulatory Info : Prescription

Registration Country : Canada

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12

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

APRACLONIDINE HYDROCHLORIDE

Brand Name : IOPIDINE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 1% BASE

Packaging :

Approval Date : 1987-12-31

Application Number : 19779

Regulatory Info : RX

Registration Country : USA

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13

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

APRACLONIDINE HYDROCHLORIDE

Brand Name : IOPIDINE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.5% BASE

Packaging :

Approval Date : 1993-07-30

Application Number : 20258

Regulatory Info : RX

Registration Country : USA

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14

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Apraclonidine Hydrochloride

Brand Name : Iopidine

Dosage Form : Eye Drop

Dosage Strength : 5mg/ml

Packaging :

Approval Date : 06-09-2002

Application Number : 2.00E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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15

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

Apraclonidine Hydrochloride

Brand Name : Iopidine

Dosage Form : Eye Drop

Dosage Strength : 5mg/ml

Packaging :

Approval Date : 06-09-2002

Application Number : 2.00E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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16

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

APRACLONIDINE HYDROCHLORIDE

Brand Name : APRACLONIDINE HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.5% BASE

Packaging :

Approval Date : 2009-03-12

Application Number : 77764

Regulatory Info : RX

Registration Country : USA

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17

Boiron Iberian Society Of Homeopath...

Country
ASCO GU
Not Confirmed
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Boiron Iberian Society Of Homeopath...

Country
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ASCO GU
Not Confirmed

Aralia Racemosa

Brand Name : Aralia Racemosa Globulos Boiron

Dosage Form : Globules

Dosage Strength :

Packaging :

Approval Date : 25-04-2022

Application Number : 86961

Regulatory Info : Authorized

Registration Country : Spain

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18

Paranova Pharmaceuticals Ab

Country
ASCO GU
Not Confirmed
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Paranova Pharmaceuticals Ab

Country
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ASCO GU
Not Confirmed

Apraclonidine Hydrochloride

Brand Name : Iopidine

Dosage Form : Eye Drop

Dosage Strength : 5mg/ml

Packaging :

Approval Date : 19-11-1999

Application Number : 2.00E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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19

Paranova Pharmaceuticals Ab

Country
ASCO GU
Not Confirmed
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Paranova Pharmaceuticals Ab

Country
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ASCO GU
Not Confirmed

Apraclonidine Hydrochloride

Brand Name : Iopidine

Dosage Form : Eye Drop

Dosage Strength : 5mg/ml

Packaging :

Approval Date : 05-10-2016

Application Number : 2.02E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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20

Novartis South Africa (Pty) Ltd

Country
ASCO GU
Not Confirmed
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Novartis South Africa (Pty) Ltd

Country
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ASCO GU
Not Confirmed

Apraclonidine

Brand Name : Iopidine 0.5%

Dosage Form : OPD

Dosage Strength : 5mg/ml

Packaging : 10X1mg/ml

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

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