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01 5Aspen Pharmacare Holdings

02 10ACS DOBFAR SPA

03 5Actavis Inc

04 6Adcock Ingram

05 2Akriti Pharmaceuticals Pvt. Ltd.

06 2Antibiotice

07 4Ascend Labs

08 3Aurobindo Pharma Limited

09 2B. Braun Medical

10 2B. Braun Melsungen AG

11 2Bausch & Lomb Incorporated

12 1Be-Tabs Pharmaceuticals

13 1Cathay Drug Company

14 2Cipla Medpro South Africa

15 2Copharma Aps

16 2DEVATS INDIA

17 3Deva Holding AS

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 14GSK

25 1Gulf Drug Company

26 2HELM Portugal

27 4Hainan Haiyao

28 1Hanlim Pharmaceuticals Inc

29 3Hikma Pharmaceuticals

30 4Hospira, Inc.

31 2INNOVATA PHARMACEUTICALS

32 1Indo Pharma

33 2Ips Farma Sl

34 2Jodas Expoim Pvt. Ltd

35 3Karo Pharma

36 1LA.FA.RE. Srl

37 3LABORATORIOS NORMON SA

38 1Laboratoires Thea

39 1Laboratoires Théa S.A.S

40 1MALESCI SpA IST.FARMACOBIOL.

41 4MIP Pharma

42 3Navamedic

43 3Nectar Lifesciences

44 3Nobel Ilac Sanayii Ve Ticaret A.S.

45 1ORIFARM GROUP AS

46 3Oethmaan Biosims

47 4Orofino Pharmaceuticals Group

48 5PAI Pharmaceutical Associates

49 4Pharmacore Inc

50 2Reach Pharmaceuticals

51 3Reig Jofre

52 2Samson Medical Technologies

53 16Sandoz B2B

54 3Specpharm

55 9Stragen Pharma SA

56 3Stravencon

57 9Sun Pharmaceutical Industries Limited

58 1TECNOPHARMA Srl

59 3Teva Pharmaceutical Industries

60 1Thea Laboratories

61 1Theon Pharmaceuticals

62 3Umedica Laboratories

63 2Unosource Pharma

64 1Vaishali Pharma Ltd

65 3Viatris

66 3Villerton Invest Said

67 4World Medicine

68 6Zeiss Pharma

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PharmaCompass

01

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

02

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

03

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

BioJapan
Not Confirmed
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BioJapan
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

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07

BioJapan
Not Confirmed
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BioJapan
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

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08

BioJapan
Not Confirmed
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BioJapan
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

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09

BioJapan
Not Confirmed
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BioJapan
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

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10

BioJapan
Not Confirmed
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BioJapan
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

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11

BioJapan
Not Confirmed
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BioJapan
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

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12

BioJapan
Not Confirmed
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BioJapan
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

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13

BioJapan
Not Confirmed
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BioJapan
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

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14

BioJapan
Not Confirmed
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BioJapan
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

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15

BioJapan
Not Confirmed
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BioJapan
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

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16

BioJapan
Not Confirmed
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BioJapan
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

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17

BioJapan
Not Confirmed
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BioJapan
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

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18

BioJapan
Not Confirmed
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BioJapan
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

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19

BioJapan
Not Confirmed
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BioJapan
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

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20

BioJapan
Not Confirmed
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BioJapan
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

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