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01 1BWX Technologies

02 1Baxter Healthcare Corporation

03 9CURIUM US LLC

04 3Cardinal Health

05 1Farmigea

06 16GE Healthcare Inc

07 1Hanlim Pharmaceuticals Inc

08 2IBA molecular

09 1SIFI

10 4Sandoz B2B

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PharmaCompass

01

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Ammonium Molybdate Tetrahydrate; Ferrous Gluconate Hydrate; Cobalt Gluconate Dihydrate; Copper Gluconate; Chromium Trichloride Hexahydrate; Manganese Gluconate; Sodium Fluoride; Sodium Iodide; Sodium Selenite Anhydrous; Zinc Gluconate Trihydrate

Brand Name : Decan

Dosage Form : Concentrate For Solution For Infusion

Dosage Strength :

Packaging :

Approval Date : 26/03/1999

Application Number : 19990326000151

Regulatory Info : Deregistered

Registration Country : Sweden

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02

VMX
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SODIUM IODIDE 123 I

Brand Name : SODIUM IODIDE I-123 ORAL SOLUTION

Dosage Form : SOLUTION

Dosage Strength : 74MBq/0.08ML

Packaging : 0.08ML IN 5ML

Approval Date :

Application Number : 2478366

Regulatory Info : Schedule C

Registration Country : Canada

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03

VMX
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SODIUM IODIDE I-123

Brand Name : SODIUM IODIDE I 123

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100uCi

Packaging :

Approval Date : 1982-05-27

Application Number : 18671

Regulatory Info : RX

Registration Country : USA

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04

VMX
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SODIUM IODIDE I-123

Brand Name : SODIUM IODIDE I 123

Dosage Form : CAPSULE;ORAL

Dosage Strength : 200uCi

Packaging :

Approval Date : 1982-05-27

Application Number : 18671

Regulatory Info : RX

Registration Country : USA

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05

VMX
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SODIUM IODIDE I-123

Brand Name : SODIUM IODIDE I 123

Dosage Form : CAPSULE;ORAL

Dosage Strength : 400uCi

Packaging :

Approval Date : 1982-05-27

Application Number : 18671

Regulatory Info : DISCN

Registration Country : USA

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06

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Sodium Iodide (123I)

Brand Name : Iodide (

Dosage Form : Injectable Solution

Dosage Strength : 37MBQ

Packaging :

Approval Date : 2009-01-19

Application Number : 70420

Regulatory Info : Authorized

Registration Country : Spain

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07

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Natriumjodid (123I)

Brand Name : Sodium Iodide [123I] Injection Curiumpharma

Dosage Form : Solution For Injection

Dosage Strength : 37MBq/ml

Packaging :

Approval Date :

Application Number :

Regulatory Info : Marketed

Registration Country : Norway

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08

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CALCIUM CHLORIDE; Potassium Iodide; Sodium Iodide

Brand Name : Polijodurato

Dosage Form :

Dosage Strength : Coll 10 Ml  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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09

VMX
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SODIUM IODIDE I-123

Brand Name : SODIUM IODIDE I 123

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100uCi

Packaging :

Approval Date : 1982-01-01

Application Number : 17630

Regulatory Info : DISCN

Registration Country : USA

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10

VMX
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SODIUM IODIDE I-123

Brand Name : SODIUM IODIDE I 123

Dosage Form : SOLUTION;ORAL

Dosage Strength : 2mCi/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 17630

Regulatory Info : DISCN

Registration Country : USA

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11

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SODIUM IODIDE I-123

Brand Name : SODIUM IODIDE I 123

Dosage Form : CAPSULE;ORAL

Dosage Strength : 200uCi

Packaging :

Approval Date : 1993-01-08

Application Number : 17630

Regulatory Info : DISCN

Registration Country : USA

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12

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Sodium Iodide (123I)

Brand Name : Iodide (

Dosage Form : Injectable Solution

Dosage Strength : 37MBQ

Packaging :

Approval Date : 2014-04-25

Application Number : 78692

Regulatory Info : Authorized

Registration Country : Spain

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13

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Potassium Iodide; Sodium Iodide

Brand Name : POSOD

Dosage Form : EYE DROP

Dosage Strength : 3MG/ML; 3MG/ML

Packaging : 10mL

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Korea

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14

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SODIUM IODIDE I-123

Brand Name : SODIUM IODIDE I 123

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100uCi

Packaging :

Approval Date : 1989-02-28

Application Number : 71909

Regulatory Info : RX

Registration Country : USA

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15

VMX
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SODIUM IODIDE I-123

Brand Name : SODIUM IODIDE I 123

Dosage Form : CAPSULE;ORAL

Dosage Strength : 200uCi

Packaging :

Approval Date : 1989-02-28

Application Number : 71910

Regulatory Info : RX

Registration Country : USA

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16

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IODIDE (SODIUM IODIDE)

Brand Name : MICRO I

Dosage Form : LIQUID

Dosage Strength : 100MCG/ML

Packaging : 10X10ML

Approval Date :

Application Number : 1974548

Regulatory Info : Ethical

Registration Country : Canada

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17

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IODIDE (SODIUM IODIDE)

Brand Name : MICRO PLUS 6 (PEDIATRIC)

Dosage Form : LIQUID

Dosage Strength : 60MCG/ML

Packaging : 10 X 10ML VIALS

Approval Date :

Application Number : 2091100

Regulatory Info : Ethical

Registration Country : Canada

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18

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IODIDE (SODIUM IODIDE)

Brand Name : MICRO+6 CONCENTRATE

Dosage Form : SOLUTION

Dosage Strength : 75MCG/ML

Packaging :

Approval Date :

Application Number : 2507587

Regulatory Info : Ethical

Registration Country : Canada

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19

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IODIDE (SODIUM IODIDE)

Brand Name : MICRO+ TE PEDIATRIC

Dosage Form : SOLUTION

Dosage Strength : 1MCG/ML

Packaging :

Approval Date :

Application Number : 2536145

Regulatory Info : Ethical

Registration Country : Canada

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20

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Sodium Iodide; calcium formate; Ascorbic Acid; Thiamine

Brand Name : Rubjovit

Dosage Form :

Dosage Strength : Coll 10 Ml  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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