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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 2Central Procurement & Supplies Unit

15 2Cipla Medpro South Africa

16 2Copharma Aps

17 2DALI Pharma GmbH

18 2DEVATS INDIA

19 3Deva Holding AS

20 2Dr. Friedrich Eberth Arzneimittel

21 4Eli Lilly

22 4Flagship Biotech International Pvt. Ltd

23 2Fresenius Kabi AB Brunna

24 2Fresenius Kabi Austria

25 3Fresenius Kabi USA

26 2Fresenius SE & Co. KGaA

27 11GSK

28 1Gulf Drug Company

29 2HELM Portugal

30 4Hainan Haiyao

31 1Hanlim Pharmaceuticals Inc

32 3Hikma Pharmaceuticals

33 4Hospira, Inc.

34 2INNOVATA PHARMACEUTICALS

35 1Indo Pharma

36 2Ips Farma Sl

37 2Jodas Expoim Pvt. Ltd

38 3Karo Pharma

39 1LA.FA.RE. Srl

40 3LABORATORIOS NORMON SA

41 1Laboratoires Thea

42 1MALESCI SpA IST.FARMACOBIOL.

43 2MIP Pharma

44 3Navamedic

45 3Nectar Lifesciences

46 3Nobel Ilac Sanayii Ve Ticaret A.S.

47 3Oethmaan Biosims

48 4Orofino Pharmaceuticals Group

49 5PAI Pharmaceutical Associates

50 4Pharmacore Inc

51 2Reach Pharmaceuticals

52 3Reig Jofre

53 2Samson Medical Technologies

54 16Sandoz B2B

55 3Specpharm

56 6Stragen Pharma SA

57 3Stravencon

58 9Sun Pharmaceutical Industries Limited

59 1TECNOPHARMA Srl

60 3Teva Pharmaceutical Industries

61 1Thea Laboratories

62 1Theon Pharmaceuticals

63 3Umedica Laboratories

64 2Unosource Pharma

65 1Vaishali Pharma Ltd

66 3Viatris

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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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VMX
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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