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01 10Sanofi

02 4Aspen Pharmacare Holdings

03 2ANDA Repository

04 2Actavis Inc

05 2Aeron Remedies

06 2Alkem Laboratories

07 2Associated Biotech

08 1Athens Life Science

09 8Aurobindo Pharma Limited

10 3BRUNO FARMACEUTICI SpA

11 2Chartwell Pharmaceuticals llc

12 5DEVATS INDIA

13 10Daiichi Sankyo

14 2Embiotic Laboratories

15 10Gracure Pharmaceuticals Limited

16 4Health Biotech

17 3Hiral Labs

18 2Jodas Expoim Pvt. Ltd

19 2Kniss Laboratories

20 3Medreich

21 5Nectar Lifesciences

22 3Nishchem International Pvt. Ltd

23 3Nobel Ilac Sanayii Ve Ticaret A.S.

24 2Orchid Pharma

25 4Pfizer Inc

26 4Pharma Dynamics

27 7RANBAXY LABORATORIES LIMITED

28 3SCHARPER SpA

29 17Sandoz B2B

30 3Scharper

31 1Shaimil Laboratories

32 1Smith & Kenner Pharmaceuticals

33 3So.Se.Pharm

34 4Sun Pharmaceutical Industries Limited

35 2Theon Pharmaceuticals

36 2Umedica Laboratories

37 4Unosource Pharma

38 7Viatris

39 6World Medicine

40 2XL Laboratories Private Limited

41 1ZOETIS MANUFACTURING ITALIA S.R.L. IT 95121 Catania

42 4Zeiss Pharma

43 6Zim Laboratories

44 3Blank

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PharmaCompass

01

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PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info :

Registration Country : Italy

Cefpodoxime

Brand Name : Orelox

Dosage Form : Cefpodoxime 0.8% 100Ml Oral Use

Dosage Strength : BB os suspe grat 100 ml 40 mg/5 ml

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Sanofi Company Banner

02

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PharmaVenue
Not Confirmed

Cefpodoxime

Brand Name : Aspen Cefpodoxime 100

Dosage Form : TAB

Dosage Strength : 100mg

Packaging : 10X1mg

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

03

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PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info :

Registration Country : Italy

Cefpodoxime

Brand Name : Orelox

Dosage Form : Cefpodoxime 100Mg 12 Combined Oral Use

Dosage Strength : 12 cpr riv 100 mg

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Sanofi Company Banner

04

arrow
PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info :

Registration Country : Italy

Cefpodoxime

Brand Name : Orelox

Dosage Form : Cefpodoxime 200Mg 6 Combined Oral Use

Dosage Strength : 6 cpr riv 200 mg

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Sanofi Company Banner

05

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PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info :

Registration Country : Italy

Cefpodoxime

Brand Name : ORELOX

Dosage Form : Granulate For Oral Suspension

Dosage Strength : 0.80%

Packaging : 100 ML 0.8% - ORAL USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Sanofi Company Banner

06

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PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info :

Registration Country : Italy

Cefpodoxime

Brand Name : ORELOX

Dosage Form : Film-Coated Tablets

Dosage Strength : 100 mg

Packaging : 12 UNITS 100 MG - ORAL USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Sanofi Company Banner

07

arrow
PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info :

Registration Country : Italy

Cefpodoxime

Brand Name : ORELOX

Dosage Form : Film-Coated Tablets

Dosage Strength : 200 mg

Packaging : 6 UNITS 200 MG - ORAL USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Sanofi Company Banner

08

arrow
PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Originator

Registration Country : South Africa

Cefpodoxime

Brand Name : Orelox 200 mg

Dosage Form : TAB

Dosage Strength : 200mg

Packaging : 10X1mg

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

Sanofi Company Banner

09

arrow
PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Originator

Registration Country : South Africa

Cefpodoxime

Brand Name : Orelox 100

Dosage Form : TAB

Dosage Strength : 100mg

Packaging : 10X1mg

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

Sanofi Company Banner

10

arrow
PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Originator

Registration Country : South Africa

Cefpodoxime

Brand Name : Orelox Junior

Dosage Form : SUS

Dosage Strength : 40mg/5ml

Packaging : 50X1mg/5ml

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

Sanofi Company Banner

11

arrow
PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Originator

Registration Country : South Africa

Cefpodozime

Brand Name : Orelox Junior

Dosage Form : SUS

Dosage Strength : 40mg/5ml

Packaging : 100X1mg/5ml

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

Sanofi Company Banner

12

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PharmaVenue
Not Confirmed

Cefpodoxime

Brand Name : Aspen Cefpodoxime 200

Dosage Form : TAB

Dosage Strength : 200mg

Packaging : 10X1mg

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

13

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PharmaVenue
Not Confirmed

Cefpodoxime

Brand Name : Aspen Cefpodoxime 40mg/5ml (Oral Suspension)

Dosage Form : SUS

Dosage Strength : 40mg/5ml

Packaging : 50X1mg/5ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

14

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PharmaVenue
Not Confirmed

Cefpodoxime

Brand Name : Aspen Cefpodoxime 40mg/5ml (Oral Suspension)

Dosage Form : SUS

Dosage Strength : 40mg/5ml

Packaging : 100X1mg/5ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

15

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 2007-11-14

Application Number : 65388

Regulatory Info : RX

Registration Country : USA

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16

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 200MG BASE

Packaging :

Approval Date : 2007-11-14

Application Number : 65388

Regulatory Info : RX

Registration Country : USA

blank

17

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 2007-06-11

Application Number : 65370

Regulatory Info : RX

Registration Country : USA

blank

18

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 200MG BASE

Packaging :

Approval Date : 2007-06-11

Application Number : 65370

Regulatory Info : RX

Registration Country : USA

blank

19

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : BANAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 1992-08-07

Application Number : 50687

Regulatory Info : DISCN

Registration Country : USA

blank

20

PharmaVenue
Not Confirmed
arrow
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PharmaVenue
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : BANAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 200MG BASE

Packaging :

Approval Date : 1992-08-07

Application Number : 50687

Regulatory Info : DISCN

Registration Country : USA

blank

21

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : BANAN

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 100MG BASE/5ML

Packaging :

Approval Date : 1992-08-07

Application Number : 50688

Regulatory Info : DISCN

Registration Country : USA

blank

22

PharmaVenue
Not Confirmed
arrow
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PharmaVenue
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : BANAN

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 50MG BASE/5ML

Packaging :

Approval Date : 1992-08-07

Application Number : 50688

Regulatory Info : DISCN

Registration Country : USA

blank

23

PharmaVenue
Not Confirmed
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PharmaVenue
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**

Packaging :

Approval Date : 1992-08-07

Application Number : 50674

Regulatory Info : DISCN

Registration Country : USA

blank

24

PharmaVenue
Not Confirmed
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PharmaVenue
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**

Packaging :

Approval Date : 1992-08-07

Application Number : 50674

Regulatory Info : DISCN

Registration Country : USA

blank

25

PharmaVenue
Not Confirmed
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PharmaVenue
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**

Packaging :

Approval Date : 1992-08-07

Application Number : 50675

Regulatory Info : DISCN

Registration Country : USA

blank

26

PharmaVenue
Not Confirmed
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PharmaVenue
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**

Packaging :

Approval Date : 1992-08-07

Application Number : 50675

Regulatory Info : DISCN

Registration Country : USA

blank

27

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 50MG BASE/5ML

Packaging :

Approval Date : 2002-05-31

Application Number : 65082

Regulatory Info : DISCN

Registration Country : USA

blank

28

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 100MG BASE/5ML

Packaging :

Approval Date : 2002-05-31

Application Number : 65082

Regulatory Info : DISCN

Registration Country : USA

blank

29

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 2003-08-20

Application Number : 65083

Regulatory Info : DISCN

Registration Country : USA

blank

30

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 200MG BASE

Packaging :

Approval Date : 2003-08-20

Application Number : 65083

Regulatory Info : DISCN

Registration Country : USA

blank