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01 2Merck & Co

02 2Pharmacil

03 3SI PHARMS

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PharmaCompass

01

Pharma, Lab & Chemical Expo
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Pharma, Lab & Chemical Expo
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ceftibutendihydrat

Brand Name : Cedax

Dosage Form : POWDER FOR ORAL SUSPENSION

Dosage Strength : 36 MG / ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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02

Pharma, Lab & Chemical Expo
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Pharma, Lab & Chemical Expo
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ceftibutendihydrat

Brand Name : Cedax

Dosage Form : HARD CAPSULES

Dosage Strength : 400 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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03

Pharma, Lab & Chemical Expo
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Pharma, Lab & Chemical Expo
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Ceftibuten Dihydrate

Brand Name : Inbuten

Dosage Form : capsule

Dosage Strength : 400MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Bangladesh

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04

Pharma, Lab & Chemical Expo
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Pharma, Lab & Chemical Expo
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Ceftibuten Dihydrate

Brand Name : Inbuten

Dosage Form : Powder for Suspension

Dosage Strength : 90MG/5ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Bangladesh

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05

SI PHARMS

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Pharma, Lab & Chemical Expo
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SI PHARMS

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CEFTIBUTEN DIHYDRATE

Brand Name : CEDAX

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 400MG BASE

Packaging :

Approval Date : 1995-12-20

Application Number : 50685

Regulatory Info : DISCN

Registration Country : USA

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06

SI PHARMS

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Pharma, Lab & Chemical Expo
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SI PHARMS

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Pharma, Lab & Chemical Expo
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CEFTIBUTEN DIHYDRATE

Brand Name : CEDAX

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 90MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1995-12-20

Application Number : 50686

Regulatory Info : DISCN

Registration Country : USA

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07

SI PHARMS

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Pharma, Lab & Chemical Expo
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SI PHARMS

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Pharma, Lab & Chemical Expo
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CEFTIBUTEN DIHYDRATE

Brand Name : CEDAX

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 180MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1995-12-20

Application Number : 50686

Regulatory Info : DISCN

Registration Country : USA

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