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

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01 3AAIPharma Services Corp.

02 4Actavis Inc

03 4Athem Pharma

04 1Chartwell Pharmaceuticals llc

05 4DURAMED PHARMS BARR

06 6GSK

07 4IVAX Pharmaceuticals Inc

08 2Lucent Biotech Ltd

09 1Quad Pharma

10 6RELIANCE FORMULATION PVT. LTD

11 4Sandoz B2B

12 4Viatris

13 1Wockhardt

14 1ZRS LABS

15 2Zota Healthcare Ltd

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01

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 1988-06-23

Application Number : 85973

Regulatory Info : DISCN

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 1996-10-25

Application Number : 40153

Regulatory Info : DISCN

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Packaging :

Approval Date : 1996-10-25

Application Number : 40153

Regulatory Info : DISCN

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 1996-10-25

Application Number : 40153

Regulatory Info : DISCN

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 1996-10-25

Application Number : 40153

Regulatory Info : DISCN

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : CONCENTRATE;ORAL

Dosage Strength : EQ 10MG BASE/ML

Packaging :

Approval Date : 1982-04-15

Application Number : 85787

Regulatory Info : DISCN

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : STELAZINE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11552

Regulatory Info : DISCN

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : STELAZINE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11552

Regulatory Info : DISCN

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : STELAZINE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 11552

Regulatory Info : DISCN

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : STELAZINE

Dosage Form : TABLET;ORAL

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

Packaging :

Approval Date : 1982-01-01

Application Number : 11552

Regulatory Info : DISCN

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : STELAZINE

Dosage Form : INJECTABLE;INJECTION

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

Packaging :

Approval Date : 1982-01-01

Application Number : 11552

Regulatory Info : DISCN

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : STELAZINE

Dosage Form : CONCENTRATE;ORAL

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

Packaging :

Approval Date : 1982-01-01

Application Number : 11552

Regulatory Info : DISCN

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 85785

Regulatory Info : RX

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 85786

Regulatory Info : RX

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 85788

Regulatory Info : RX

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 85789

Regulatory Info : RX

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 1997-07-07

Application Number : 40209

Regulatory Info : RX

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Packaging :

Approval Date : 1997-07-07

Application Number : 40209

Regulatory Info : RX

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 1997-07-07

Application Number : 40209

Regulatory Info : RX

Registration Country : USA

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TRIFLUOPERAZINE HYDROCHLORIDE

Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 1997-07-07

Application Number : 40209

Regulatory Info : RX

Registration Country : USA

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