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01 3ANI PHARMS

02 1BELCHER

03 1CHARTWELL RX

04 1CITRUSPHRMA

05 2CMP PHARMA INC

06 1CONCORDIA

07 1EPIC PHARMA LLC

08 1HIKMA

09 2KVK TECH

10 1MORTON GROVE

11 2NUVO PHARMS INC

12 1PAI HOLDINGS PHARM

13 1ROXANE

14 1UPSHER SMITH LABS

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PharmaCompass

01

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

SODIUM POLYSTYRENE SULFONATE

Brand Name : KIONEX

Dosage Form : SUSPENSION;ORAL, RECTAL

Dosage Strength : 15GM/60ML

Approval Date : 2007-09-17

Application Number : 40028

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

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02

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

SODIUM POLYSTYRENE SULFONATE

Brand Name : KIONEX

Dosage Form : POWDER;ORAL, RECTAL

Dosage Strength : 454GM/BOT

Approval Date : 1998-02-06

Application Number : 40029

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

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03

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

SODIUM POLYSTYRENE SULFONATE

Brand Name : SPS

Dosage Form : SUSPENSION;ORAL, RECTAL

Dosage Strength : 15GM/60ML

Approval Date : 1982-12-08

Application Number : 87859

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AA

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04

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

SODIUM POLYSTYRENE SULFONATE

Brand Name : KAYEXALATE

Dosage Form : POWDER;ORAL, RECTAL

Dosage Strength : 453.6GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 11287

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

SODIUM POLYSTYRENE SULFONATE

Brand Name : KALEXATE

Dosage Form : POWDER;ORAL, RECTAL

Dosage Strength : 454GM/BOT

Approval Date : 2009-03-30

Application Number : 40905

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

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06

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

SODIUM POLYSTYRENE SULFONATE

Brand Name : KALEXATE

Dosage Form : POWDER;ORAL, RECTAL

Dosage Strength : 15GM/BOT

Approval Date : 2015-04-03

Application Number : 40905

RX/OTC/DISCN : RX

RLD : No

TE Code :

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07

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

SODIUM POLYSTYRENE SULFONATE

Brand Name : SODIUM POLYSTYRENE SULFONATE

Dosage Form : SUSPENSION;ORAL, RECTAL

Dosage Strength : 15GM/60ML

Approval Date : 1984-09-11

Application Number : 88717

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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08

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

SODIUM POLYSTYRENE SULFONATE

Brand Name : SODIUM POLYSTYRENE SULFONATE

Dosage Form : POWDER;ORAL, RECTAL

Dosage Strength : 453.6GM/BOT

Approval Date : 1984-09-11

Application Number : 88786

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

SODIUM POLYSTYRENE SULFONATE

Brand Name : SODIUM POLYSTYRENE SULFONATE

Dosage Form : SUSPENSION;ORAL, RECTAL

Dosage Strength : 15GM/60ML

Approval Date : 1983-11-17

Application Number : 88453

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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10

CITRUSPHRMA

Country
Fi Europe 2024
Not Confirmed
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CITRUSPHRMA

Country
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Fi Europe 2024
Not Confirmed

SODIUM POLYSTYRENE SULFONATE

Brand Name : SODIUM POLYSTYRENE SULFONATE

Dosage Form : POWDER;ORAL, RECTAL

Dosage Strength : 454GM/BOT

Approval Date : 2008-12-03

Application Number : 40909

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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