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01 13BRACCO

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PharmaCompass

01

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BARIUM SULFATE

Brand Name : E-Z-HD

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : 98% (334GM/BOT)

Approval Date : 2016-01-11

Application Number : 208036

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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02

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BARIUM SULFATE

Brand Name : E-Z-PAQUE

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : 96% (169GM/BOT)

Approval Date : 2017-04-07

Application Number : 208036

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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03

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BARIUM SULFATE

Brand Name : E-Z-CAT DRY

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : 40% (9GM/POUCH)

Approval Date : 2017-01-03

Application Number : 208036

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

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BARIUM SULFATE

Brand Name : VARIBAR THIN LIQUID

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : 81% (120GM/BOT)

Approval Date : 2019-04-30

Application Number : 208036

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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05

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BARIUM SULFATE

Brand Name : READI-CAT 2

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 2% (9GM/BOT)

Approval Date : 2016-01-15

Application Number : 208143

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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06

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BARIUM SULFATE

Brand Name : READI-CAT 2 SMOOTHIE

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 2% (9GM/BOT)

Approval Date : 2016-01-15

Application Number : 208143

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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07

PackExpo
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BARIUM SULFATE

Brand Name : LIQUID E-Z-PAQUE

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 60% (213GM/BOT)

Approval Date : 2017-03-01

Application Number : 208143

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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08

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BARIUM SULFATE

Brand Name : VARIBAR NECTAR

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 40% (96GM/240ML)

Approval Date : 2017-07-07

Application Number : 208143

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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09

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BARIUM SULFATE

Brand Name : TAGITOL V

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 40% (8GM/BOT)

Approval Date : 2017-08-04

Application Number : 208143

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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10

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BARIUM SULFATE

Brand Name : VARIBAR THIN HONEY

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 40% (100GM/250ML)

Approval Date : 2018-01-23

Application Number : 208143

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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