Please Wait
Applying Filters...
Menu
$ API Ref.Price (USD/KG) : 202Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 5Aspen Pharmacare Holdings

02 10ACS DOBFAR SPA

03 5Actavis Inc

04 6Adcock Ingram

05 2Akriti Pharmaceuticals Pvt. Ltd.

06 4Alkem Laboratories (Pty) Ltd

07 2Antibiotice SA

08 3Aurobindo Pharma Limited

09 2Axapharm

10 2B. Braun Medical

11 2B. Braun Melsungen AG

12 1Be-Tabs Pharmaceuticals

13 1Cathay Drug Company

14 2Cipla Medpro South Africa

15 2DEVATS INDIA

16 3Deva Holding AS

17 3Do Fullerton Invest SA

18 4Eli Lilly

19 4Flagship Biotech International Pvt. Ltd

20 4Fresenius Kabi AB Brunna

21 2Fresenius Kabi Austria

22 3Fresenius Kabi USA

23 2Fresenius SE & Co. KGaA

24 21GSK

25 1Gulf Drug Company

26 4Hainan Haiyao

27 1Hanlim Pharmaceuticals Inc

28 3Hikma Pharmaceuticals

29 4Hospira, Inc.

30 2INNOVATA PHARMACEUTICALS

31 1Indo Pharma

32 2Jodas Expoim Pvt. Ltd

33 1LA.FA.RE. Srl

34 1Laboratoires Thea

35 1Laboratoires Théa S.A.S

36 1MALESCI SpA IST.FARMACOBIOL.

37 4MIP Pharma

38 2Mepha Pharma

39 3Nectar Lifesciences

40 3Nobel Ilac Sanayii Ve Ticaret A.S.

41 1ORIFARM GROUP AS

42 3Oethmaan Biosims

43 4Orofino Pharmaceuticals Group

44 5PAI Pharmaceutical Associates

45 4Pharmacore Inc

46 2Reach Pharmaceuticals

47 2Samson Medical Technologies

48 12Sandoz B2B

49 3Specpharm

50 2Spirig Healthcare

51 9Stragen Pharma SA

52 3Stravencon Limited

53 9Sun Pharmaceutical Industries Limited

54 1TECNOPHARMA Srl

55 3Teva Pharmaceutical Industries

56 1Theon Pharmaceuticals

57 3Umedica Laboratories

58 2Unosource Pharma

59 1Vaishali Pharma Ltd

60 3Viatris

61 3Villerton Invest Said

62 4World Medicine

63 6Zeiss Pharma

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

arrow
ELCC
Not Confirmed

cefuroxime

Brand Name : Zinnat

Dosage Form :

Dosage Strength :

Packaging : 20

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

Aspen API Comapny Banner

02

arrow
ELCC
Not Confirmed

cefuroxime

Brand Name : Zinnat

Dosage Form :

Dosage Strength :

Packaging : 20

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

Aspen API Comapny Banner

03

arrow
ELCC
Not Confirmed

Cefuroxime

Brand Name : Aspen Cefuroxime 1,5 G

Dosage Form : INJ

Dosage Strength : 125mg/ml

Packaging : 15X10mg/ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

04

arrow
ELCC
Not Confirmed

Cefuroxime

Brand Name : Aspen Cefuroxime 750 Mg

Dosage Form : INJ

Dosage Strength : 125mg/ml

Packaging : 6X10mg/ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

05

arrow
ELCC
Not Confirmed

Cefuroxime

Brand Name : Aspen Cefuroxime 250 Mg

Dosage Form : INJ

Dosage Strength : 125mg/ml

Packaging : 2X10mg/ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

06

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : KEFUROX

Dosage Form : INJECTABLE;INTRAMUSCULAR, INTRAVENOUS

Dosage Strength : EQ 750MG BASE/VIAL

Packaging :

Approval Date : 1986-01-10

Application Number : 62591

Regulatory Info : DISCN

Registration Country : USA

blank

07

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : KEFUROX

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1.5GM BASE/VIAL

Packaging :

Approval Date : 1986-01-10

Application Number : 62591

Regulatory Info : DISCN

Registration Country : USA

blank

08

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : KEFUROX

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 7.5GM BASE/VIAL

Packaging :

Approval Date : 1987-12-17

Application Number : 62591

Regulatory Info : DISCN

Registration Country : USA

blank

09

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : CEFUROXIME SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 7.5GM BASE/VIAL

Packaging :

Approval Date : 1997-05-30

Application Number : 64124

Regulatory Info : DISCN

Registration Country : USA

blank

10

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : CEFUROXIME SODIUM

Dosage Form : INJECTABLE;INTRAMUSCULAR, INTRAVENOUS

Dosage Strength : EQ 750MG BASE/VIAL

Packaging :

Approval Date : 1997-05-30

Application Number : 64125

Regulatory Info : RX

Registration Country : USA

blank

11

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : CEFUROXIME SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1.5GM BASE/VIAL

Packaging :

Approval Date : 1997-05-30

Application Number : 64125

Regulatory Info : RX

Registration Country : USA

blank

12

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : CEFUROXIME SODIUM

Dosage Form : INJECTABLE;INTRAMUSCULAR, INTRAVENOUS

Dosage Strength : EQ 750MG BASE/VIAL

Packaging :

Approval Date : 1993-02-26

Application Number : 64035

Regulatory Info : DISCN

Registration Country : USA

blank

13

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : CEFUROXIME SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1.5GM BASE/VIAL

Packaging :

Approval Date : 1993-02-26

Application Number : 64035

Regulatory Info : DISCN

Registration Country : USA

blank

14

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : CEFUROXIME SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 7.5GM BASE/VIAL

Packaging :

Approval Date : 1993-02-26

Application Number : 64036

Regulatory Info : DISCN

Registration Country : USA

blank

15

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : CEFUROXIME AND DEXTROSE IN DUPLEX CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 750MG BASE/VIAL

Packaging :

Approval Date : 2001-02-21

Application Number : 50780

Regulatory Info : DISCN

Registration Country : USA

blank

16

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : CEFUROXIME AND DEXTROSE IN DUPLEX CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1.5GM BASE/VIAL

Packaging :

Approval Date : 2001-02-21

Application Number : 50780

Regulatory Info : DISCN

Registration Country : USA

blank

17

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : KEFUROX IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 750MG BASE/VIAL

Packaging :

Approval Date : 1986-01-10

Application Number : 62590

Regulatory Info : DISCN

Registration Country : USA

blank

18

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : KEFUROX IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1.5GM BASE/VIAL

Packaging :

Approval Date : 1986-01-10

Application Number : 62590

Regulatory Info : DISCN

Registration Country : USA

blank

19

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : KEFUROX

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 750MG BASE/VIAL

Packaging :

Approval Date : 1986-01-10

Application Number : 62592

Regulatory Info : DISCN

Registration Country : USA

blank

20

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : KEFUROX

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1.5GM BASE/VIAL

Packaging :

Approval Date : 1986-01-10

Application Number : 62592

Regulatory Info : DISCN

Registration Country : USA

blank

21

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : CEFUROXIME SODIUM

Dosage Form : INJECTABLE;INTRAMUSCULAR, INTRAVENOUS

Dosage Strength : EQ 750MG BASE/VIAL

Packaging :

Approval Date : 2001-05-30

Application Number : 65001

Regulatory Info : DISCN

Registration Country : USA

blank

22

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : CEFUROXIME SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1.5GM BASE/VIAL

Packaging :

Approval Date : 2001-05-30

Application Number : 65001

Regulatory Info : DISCN

Registration Country : USA

blank

23

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : ZINACEF

Dosage Form : INJECTABLE;INTRAMUSCULAR, INTRAVENOUS

Dosage Strength : EQ 750MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1983-10-19

Application Number : 50558

Regulatory Info : DISCN

Registration Country : USA

blank

24

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : ZINACEF

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1.5GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1983-10-19

Application Number : 50558

Regulatory Info : DISCN

Registration Country : USA

blank

25

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : ZINACEF

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 7.5GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1986-10-23

Application Number : 50558

Regulatory Info : DISCN

Registration Country : USA

blank

26

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : ZINACEF IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 15MG BASE/ML

Packaging :

Approval Date : 1989-04-28

Application Number : 50643

Regulatory Info : DISCN

Registration Country : USA

blank

27

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : ZINACEF IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 30MG BASE/ML

Packaging :

Approval Date : 1989-04-28

Application Number : 50643

Regulatory Info : DISCN

Registration Country : USA

blank

28

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : CEFUROXIME SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 7.5GM BASE/VIAL

Packaging :

Approval Date : 1998-04-16

Application Number : 64191

Regulatory Info : DISCN

Registration Country : USA

blank

29

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : CEFUROXIME SODIUM

Dosage Form : INJECTABLE;INTRAMUSCULAR, INTRAVENOUS

Dosage Strength : EQ 1.5GM BASE/VIAL

Packaging :

Approval Date : 1998-04-16

Application Number : 64192

Regulatory Info : DISCN

Registration Country : USA

blank

30

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CEFUROXIME SODIUM

Brand Name : CEFUROXIME SODIUM

Dosage Form : INJECTABLE;INTRAMUSCULAR, INTRAVENOUS

Dosage Strength : EQ 750MG BASE/VIAL

Packaging :

Approval Date : 1998-04-16

Application Number : 64192

Regulatory Info : DISCN

Registration Country : USA

blank