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01 2ALKEM LABS LTD

02 2ANDA REPOSITORY

03 2AUROBINDO PHARMA

04 2AUROBINDO PHARMA LTD

05 2CHARTWELL RX

06 4PHARMACIA AND UPJOHN

07 2SANDOZ

08 4SANKYO

09 4SUN PHARM INDS LTD

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PharmaCompass

01

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : BANAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 100MG BASE

Approval Date : 1992-08-07

Application Number : 50687

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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02

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : BANAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 200MG BASE

Approval Date : 1992-08-07

Application Number : 50687

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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03

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : BANAN

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 100MG BASE/5ML

Approval Date : 1992-08-07

Application Number : 50688

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : BANAN

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 50MG BASE/5ML

Approval Date : 1992-08-07

Application Number : 50688

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : VANTIN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1992-08-07

Application Number : 50674

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : VANTIN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1992-08-07

Application Number : 50674

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

07

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : VANTIN

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 50MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1992-08-07

Application Number : 50675

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : VANTIN

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 100MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1992-08-07

Application Number : 50675

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

09

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 50MG BASE/5ML

Approval Date : 2002-05-31

Application Number : 65082

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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10

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 100MG BASE/5ML

Approval Date : 2002-05-31

Application Number : 65082

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank