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List of All Manufacturers & Suppliers of DSSTox_CID_29360 Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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$ API Ref.Price (USD/KG) : 491Xls
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01 9ANI Pharmaceuticals Inc

02 18Actavis Inc

03 4Avet Pharmaceuticals

04 7Chartwell Pharmaceuticals llc

05 2Epic Pharma. LLC.

06 4Mutual Pharmaceutical Company, Inc.

07 9Novartis Pharmaceuticals Corporation

08 2PHARM ASSOC

09 7Par Pharmaceutical

10 6ROXANE

11 3SUPERPHARM

12 2Sandoz B2B

13 7Sun Pharmaceutical Industries Limited

14 8Viatris

15 4West-ward Pharmaceutical Corp

16 2Wockhardt

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THIORIDAZINE HYDROCHLORIDE

Brand Name : THIORIDAZINE HYDROCHLORIDE

Dosage Form : CONCENTRATE;ORAL

Dosage Strength : 30MG/ML

Packaging :

Approval Date : 1983-04-26

Application Number : 87766

Regulatory Info : DISCN

Registration Country : USA

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THIORIDAZINE HYDROCHLORIDE

Brand Name : THIORIDAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 1983-08-30

Application Number : 88131

Regulatory Info : DISCN

Registration Country : USA

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THIORIDAZINE HYDROCHLORIDE

Brand Name : THIORIDAZINE HYDROCHLORIDE

Dosage Form : CONCENTRATE;ORAL

Dosage Strength : 30MG/ML

Packaging :

Approval Date : 1996-08-16

Application Number : 40125

Regulatory Info : DISCN

Registration Country : USA

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04

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THIORIDAZINE HYDROCHLORIDE

Brand Name : THIORIDAZINE HYDROCHLORIDE

Dosage Form : CONCENTRATE;ORAL

Dosage Strength : 100MG/ML

Packaging :

Approval Date : 1996-08-16

Application Number : 40126

Regulatory Info : DISCN

Registration Country : USA

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THIORIDAZINE HYDROCHLORIDE

Brand Name : THIORIDAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG

Packaging :

Approval Date : 1983-11-18

Application Number : 87264

Regulatory Info : DISCN

Registration Country : USA

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THIORIDAZINE HYDROCHLORIDE

Brand Name : MELLARIL

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11808

Regulatory Info : DISCN

Registration Country : USA

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THIORIDAZINE HYDROCHLORIDE

Brand Name : MELLARIL

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11808

Regulatory Info : DISCN

Registration Country : USA

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08

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THIORIDAZINE HYDROCHLORIDE

Brand Name : MELLARIL

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11808

Regulatory Info : DISCN

Registration Country : USA

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09

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THIORIDAZINE HYDROCHLORIDE

Brand Name : MELLARIL

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11808

Regulatory Info : DISCN

Registration Country : USA

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10

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THIORIDAZINE HYDROCHLORIDE

Brand Name : MELLARIL

Dosage Form : CONCENTRATE;ORAL

Dosage Strength : 30MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11808

Regulatory Info : DISCN

Registration Country : USA

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11

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THIORIDAZINE HYDROCHLORIDE

Brand Name : MELLARIL

Dosage Form : TABLET;ORAL

Dosage Strength : 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11808

Regulatory Info : DISCN

Registration Country : USA

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THIORIDAZINE HYDROCHLORIDE

Brand Name : MELLARIL

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11808

Regulatory Info : DISCN

Registration Country : USA

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THIORIDAZINE HYDROCHLORIDE

Brand Name : MELLARIL

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11808

Regulatory Info : DISCN

Registration Country : USA

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14

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THIORIDAZINE HYDROCHLORIDE

Brand Name : MELLARIL

Dosage Form : CONCENTRATE;ORAL

Dosage Strength : 100MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11808

Regulatory Info : DISCN

Registration Country : USA

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PHARM ASSOC

U.S.A
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PHARM ASSOC

U.S.A
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THIORIDAZINE HYDROCHLORIDE

Brand Name : THIORIDAZINE HYDROCHLORIDE

Dosage Form : CONCENTRATE;ORAL

Dosage Strength : 30MG/ML

Packaging :

Approval Date : 1997-08-28

Application Number : 40187

Regulatory Info : DISCN

Registration Country : USA

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16

PHARM ASSOC

U.S.A
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PHARM ASSOC

U.S.A
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THIORIDAZINE HYDROCHLORIDE

Brand Name : THIORIDAZINE HYDROCHLORIDE

Dosage Form : CONCENTRATE;ORAL

Dosage Strength : 100MG/ML

Packaging :

Approval Date : 1998-05-29

Application Number : 40213

Regulatory Info : DISCN

Registration Country : USA

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THIORIDAZINE HYDROCHLORIDE

Brand Name : THIORIDAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1983-11-18

Application Number : 88004

Regulatory Info : RX

Registration Country : USA

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THIORIDAZINE HYDROCHLORIDE

Brand Name : THIORIDAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 1983-03-15

Application Number : 88004

Regulatory Info : RX

Registration Country : USA

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THIORIDAZINE HYDROCHLORIDE

Brand Name : THIORIDAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG

Packaging :

Approval Date : 1983-03-15

Application Number : 88004

Regulatory Info : RX

Registration Country : USA

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THIORIDAZINE HYDROCHLORIDE

Brand Name : THIORIDAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1983-03-15

Application Number : 88004

Regulatory Info : RX

Registration Country : USA

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