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01 1ACTAVIS MID ATLANTIC

02 1ALPHARMA US PHARMS

03 9ANI PHARMS

04 7CHARTWELL RX

05 2EPIC PHARMA LLC

06 4HERITAGE PHARMA AVET

07 4MUTUAL PHARM

08 8MYLAN

09 9NOVARTIS

10 7PAR PHARM

11 2PHARM ASSOC

12 6ROXANE

13 2SANDOZ

14 7SUN PHARM INDUSTRIES

15 3SUPERPHARM

16 13WATSON LABS

17 3WATSON LABS TEVA

18 4WEST WARD

19 2WOCKHARDT

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PharmaCompass

01

American Pharma Summit
Not Confirmed
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American Pharma Summit
Not Confirmed

THIORIDAZINE HYDROCHLORIDE

Brand Name : THIORIDAZINE HYDROCHLORIDE

Dosage Form : CONCENTRATE;ORAL

Dosage Strength : 30MG/ML

Approval Date : 1996-08-16

Application Number : 40125

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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02

American Pharma Summit
Not Confirmed
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American Pharma Summit
Not Confirmed

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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 11808

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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03

American Pharma Summit
Not Confirmed
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American Pharma Summit
Not Confirmed

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Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 11808

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

American Pharma Summit
Not Confirmed
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American Pharma Summit
Not Confirmed

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Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 11808

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

American Pharma Summit
Not Confirmed
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American Pharma Summit
Not Confirmed

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**

Approval Date : 1982-01-01

Application Number : 11808

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

06

American Pharma Summit
Not Confirmed
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American Pharma Summit
Not Confirmed

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**

Approval Date : 1982-01-01

Application Number : 11808

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

07

American Pharma Summit
Not Confirmed
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American Pharma Summit
Not Confirmed

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**

Approval Date : 1982-01-01

Application Number : 11808

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

American Pharma Summit
Not Confirmed
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American Pharma Summit
Not Confirmed

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**

Approval Date : 1982-01-01

Application Number : 11808

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

American Pharma Summit
Not Confirmed
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American Pharma Summit
Not Confirmed

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**

Approval Date : 1982-01-01

Application Number : 11808

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

10

American Pharma Summit
Not Confirmed
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American Pharma Summit
Not Confirmed

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**

Approval Date : 1982-01-01

Application Number : 11808

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank