Please Wait
Applying Filters...
Menu
$ API Ref.Price (USD/KG) : 159Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 6Sanofi

02 2ANDA Repository

03 2Actavis Inc

04 4Adcock Ingram

05 2Aeron Remedies

06 2Alkem Laboratories

07 4Ascend Labs

08 2Associated Biotech

09 1Athens Life Science

10 8Aurobindo Pharma Limited

11 3BRUNO FARMACEUTICI SpA

12 2Chartwell Pharmaceuticals llc

13 4Clinigen Group

14 5DEVATS INDIA

15 10Daiichi Sankyo

16 2Embiotic Laboratories

17 10Gracure Pharmaceuticals Limited

18 4Health Biotech

19 3Hiral Labs

20 2Jodas Expoim Pvt. Ltd

21 2Kniss Laboratories

22 3Medreich

23 5Nectar Lifesciences

24 3Nishchem International Pvt. Ltd

25 3Nobel Ilac Sanayii Ve Ticaret A.S.

26 2Orchid Pharma

27 4Pfizer Inc

28 4Pharma Dynamics

29 3SCHARPER SpA

30 17Sandoz B2B

31 3Scharper

32 1Shaimil Laboratories

33 1Smith & Kenner Pharmaceuticals

34 3So.Se.Pharm

35 11Sun Pharmaceutical Industries Limited

36 2Theon Pharmaceuticals

37 2Tossvet Pharmaceuticals

38 2Umedica Laboratories

39 4Unosource Pharma

40 7Viatris

41 6World Medicine

42 2XL Laboratories Private Limited

43 1ZOETIS MANUFACTURING ITALIA S.R.L. IT 95121 Catania

44 4Zeiss Pharma

45 6Zim Laboratories

46 3Blank

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

  • 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

  • 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

03

  • 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

04

  • 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

05

  • 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

06

  • 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

07

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 2022-05-18

Application Number : 210568

Regulatory Info : RX

Registration Country : USA

blank

08

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 200MG BASE

Packaging :

Approval Date : 2022-05-18

Application Number : 210568

Regulatory Info : RX

Registration Country : USA

blank

09

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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

blank

10

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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

11

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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

12

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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

13

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 50MG BASE/5ML

Packaging :

Approval Date : 2007-06-08

Application Number : 65409

Regulatory Info : RX

Registration Country : USA

blank

14

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 100MG BASE/5ML

Packaging :

Approval Date : 2007-06-08

Application Number : 65409

Regulatory Info : RX

Registration Country : USA

blank

15

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 50MG BASE/5ML

Packaging :

Approval Date : 2009-01-14

Application Number : 90031

Regulatory Info : DISCN

Registration Country : USA

blank

16

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 100MG BASE/5ML

Packaging :

Approval Date : 2009-01-14

Application Number : 90031

Regulatory Info : DISCN

Registration Country : USA

blank

17

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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

18

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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

19

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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

20

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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

21

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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

22

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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

23

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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

24

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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

25

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 2008-05-28

Application Number : 65462

Regulatory Info : RX

Registration Country : USA

blank

26

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

CEFPODOXIME PROXETIL

Brand Name : CEFPODOXIME PROXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 200MG BASE

Packaging :

Approval Date : 2008-05-28

Application Number : 65462

Regulatory Info : RX

Registration Country : USA

blank

27

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
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