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01 1GUERBET

02 6Mallinckrodt Pharmaceuticals

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PharmaCompass

01

Antibody Engineering
Not Confirmed
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Antibody Engineering
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IOTHALAMATE MEGLUMINE

Brand Name : CYSTO-CONRAY II

Dosage Form : SOLUTION

Dosage Strength : 172MG/ML

Packaging : 250/500ML

Approval Date :

Application Number : 397466

Regulatory Info : Ethical

Registration Country : Canada

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02

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

IOTHALAMATE MEGLUMINE

Brand Name : CONRAY

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 60%

Packaging :

Approval Date : 1982-01-01

Application Number : 13295

Regulatory Info : RX

Registration Country : USA

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03

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

IOTHALAMATE MEGLUMINE

Brand Name : CONRAY 43

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 43%

Packaging :

Approval Date : 1982-01-01

Application Number : 13295

Regulatory Info : DISCN

Registration Country : USA

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04

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

IOTHALAMATE MEGLUMINE; IOTHALAMATE SODIUM

Brand Name : VASCORAY

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 52%;26%

Packaging :

Approval Date : 1982-01-01

Application Number : 16783

Regulatory Info : DISCN

Registration Country : USA

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05

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

IOTHALAMATE MEGLUMINE

Brand Name : CONRAY 30

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 30%

Packaging :

Approval Date : 1982-01-01

Application Number : 16983

Regulatory Info : DISCN

Registration Country : USA

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06

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

IOTHALAMATE MEGLUMINE

Brand Name : CYSTO-CONRAY

Dosage Form : Solution; Intravesical, Ureteral

Dosage Strength : 43%

Packaging :

Approval Date :

Application Number : 17057

Regulatory Info :

Registration Country : USA

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07

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

IOTHALAMATE MEGLUMINE

Brand Name : CYSTO-CONRAY II

Dosage Form : SOLUTION;INTRAVESICAL

Dosage Strength : 17.2%

Packaging :

Approval Date : 1982-01-01

Application Number : 17057

Regulatory Info : RX

Registration Country : USA

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