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01 3Pharmathen SA

02 3ANDA Repository

03 2ANI Pharmaceuticals Inc

04 2Actor Pharma

05 2Adcock Ingram

06 2Aeron Remedies

07 2Alkem Laboratories

08 2Ananta Medicare

09 4Apotex Inc

10 1Athens Life Science

11 2Auro Pharma Inc

12 6Aurobindo Pharma Limited

13 2Aurogen South Africa (Pty) Ltd

14 2B. Braun Melsungen AG

15 1BIDIPHAR

16 1Be-Tabs Pharmaceuticals

17 2CRINOS SpA

18 3Chartwell Pharmaceuticals llc

19 4DEVATS INDIA

20 1EG Spa

21 3Farabi Pharmaceutical

22 2Fosun Pharmaceutical

23 1Future Pharma

24 9GSK

25 2Health Biotech

26 2Hikma Pharmaceuticals

27 1Hiral Labs

28 1IBN Savio

29 2Jodas Expoim Pvt. Ltd

30 2Lupin Ltd

31 4MALESCI SpA IST.FARMACOBIOL.

32 2MS Pharma

33 2Malesci Istituto Farmacobiologico

34 3Medreich

35 1NATIONAL BIOCHEMISTRY INSTITUTE SAVIO SRL

36 4Nectar Lifesciences

37 2Nobel Ilac Sanayii Ve Ticaret A.S.

38 5Orchid Pharma

39 3RANBAXY LABORATORIES LIMITED

40 8Sandoz B2B

41 1Shaimil Laboratories

42 1Smith & Kenner Pharmaceuticals

43 5Sun Pharmaceutical Industries Limited

44 2Synoptis Pharma

45 1Tecnopharma

46 2Theon Pharmaceuticals

47 2Umedica Laboratories

48 1Unicorn Pharmaceuticals

49 2Unosource Pharma

50 2Viatris

51 3XL Laboratories Private Limited

52 2Zeiss Pharma

53 6Zim Laboratories

54 2Éticos

55 83Blank

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PharmaCompass

01

arrow
Fi Europe 2024
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.

Regulatory Info : EU Approved

Registration Country : Greece

Cefuroxime Axetil

Brand Name :

Dosage Form : Film Coated Tablet

Dosage Strength : 125MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : EU Approved

Registration Country : Greece

Pharmathen

02

arrow
Fi Europe 2024
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.

Regulatory Info : EU Approved

Registration Country : Greece

Cefuroxime Axetil

Brand Name :

Dosage Form : Film Coated Tablet

Dosage Strength : 250MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : EU Approved

Registration Country : Greece

Pharmathen

03

arrow
Fi Europe 2024
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.

Regulatory Info : EU Approved

Registration Country : Greece

Cefuroxime Axetil

Brand Name :

Dosage Form : Film Coated Tablet

Dosage Strength : 500MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : EU Approved

Registration Country : Greece

Pharmathen

04

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 2004-10-18

Application Number : 65190

Regulatory Info : DISCN

Registration Country : USA

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05

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 500MG BASE

Packaging :

Approval Date : 2004-10-18

Application Number : 65190

Regulatory Info : DISCN

Registration Country : USA

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06

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 2002-10-02

Application Number : 65069

Regulatory Info : RX

Registration Country : USA

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07

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 500MG BASE

Packaging :

Approval Date : 2002-10-02

Application Number : 65069

Regulatory Info : RX

Registration Country : USA

blank

08

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 125MG BASE

Packaging :

Approval Date : 2006-03-29

Application Number : 65308

Regulatory Info : RX

Registration Country : USA

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09

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 2006-03-29

Application Number : 65308

Regulatory Info : RX

Registration Country : USA

blank

10

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 500MG BASE

Packaging :

Approval Date : 2006-03-29

Application Number : 65308

Regulatory Info : RX

Registration Country : USA

blank

11

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 125MG BASE

Packaging :

Approval Date : 2005-07-29

Application Number : 65166

Regulatory Info : RX

Registration Country : USA

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12

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 2005-07-29

Application Number : 65166

Regulatory Info : RX

Registration Country : USA

blank

13

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 500MG BASE

Packaging :

Approval Date : 2005-07-29

Application Number : 65166

Regulatory Info : RX

Registration Country : USA

blank

14

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 2003-10-28

Application Number : 65126

Regulatory Info : DISCN

Registration Country : USA

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15

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 500MG BASE

Packaging :

Approval Date : 2003-10-28

Application Number : 65126

Regulatory Info : DISCN

Registration Country : USA

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16

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFTIN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1987-12-28

Application Number : 50605

Regulatory Info : DISCN

Registration Country : USA

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17

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFTIN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1987-12-28

Application Number : 50605

Regulatory Info : DISCN

Registration Country : USA

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18

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFTIN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1987-12-28

Application Number : 50605

Regulatory Info : DISCN

Registration Country : USA

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19

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFTIN

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 125MG BASE/5ML

Packaging :

Approval Date : 1994-06-30

Application Number : 50672

Regulatory Info : DISCN

Registration Country : USA

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20

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFTIN

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 250MG BASE/5ML

Packaging :

Approval Date : 1997-04-29

Application Number : 50672

Regulatory Info : DISCN

Registration Country : USA

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21

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME

Brand Name : CEFUROXIME

Dosage Form : Injectable; Injection

Dosage Strength : 1.5G/20ML

Packaging :

Approval Date :

Application Number : 65048

Regulatory Info :

Registration Country : USA

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22

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME

Brand Name : CEFUROXIME

Dosage Form : Injectable; Injection

Dosage Strength : 1.5G/100ML

Packaging :

Approval Date :

Application Number : 65048

Regulatory Info :

Registration Country : USA

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23

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 2003-07-25

Application Number : 65135

Regulatory Info : RX

Registration Country : USA

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24

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 500MG BASE

Packaging :

Approval Date : 2003-07-25

Application Number : 65135

Regulatory Info : RX

Registration Country : USA

blank

25

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 500MG BASE

Packaging :

Approval Date : 2002-02-15

Application Number : 65043

Regulatory Info : DISCN

Registration Country : USA

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26

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 2002-02-15

Application Number : 65043

Regulatory Info : DISCN

Registration Country : USA

blank

27

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 125MG BASE

Packaging :

Approval Date : 2002-02-15

Application Number : 65043

Regulatory Info : DISCN

Registration Country : USA

blank

28

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 125MG BASE

Packaging :

Approval Date : 2003-04-25

Application Number : 65118

Regulatory Info : DISCN

Registration Country : USA

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29

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 2003-04-25

Application Number : 65118

Regulatory Info : DISCN

Registration Country : USA

blank

30

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

CEFUROXIME AXETIL

Brand Name : CEFUROXIME AXETIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 500MG BASE

Packaging :

Approval Date : 2003-04-25

Application Number : 65118

Regulatory Info : DISCN

Registration Country : USA

blank