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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 2Cipla Medpro South Africa

14 2DEVATS INDIA

15 3Deva Holding AS

16 3Do Fullerton Invest SA

17 4Eli Lilly

18 4Flagship Biotech International Pvt. Ltd

19 4Fresenius Kabi AB Brunna

20 2Fresenius Kabi Austria

21 3Fresenius Kabi USA

22 2Fresenius SE & Co. KGaA

23 21GSK

24 1Gulf Drug Company

25 4Hainan Haiyao

26 1Hanlim Pharmaceuticals Inc

27 3Hikma Pharmaceuticals

28 4Hospira, Inc.

29 2INNOVATA PHARMACEUTICALS

30 1Indo Pharma

31 2Jodas Expoim Pvt. Ltd

32 1LA.FA.RE. Srl

33 1Laboratoires Thea

34 1Laboratoires Théa S.A.S

35 1MALESCI SpA IST.FARMACOBIOL.

36 4MIP Pharma

37 2Mepha Pharma

38 3Nectar Lifesciences

39 3Nobel Ilac Sanayii Ve Ticaret A.S.

40 1ORIFARM GROUP AS

41 3Oethmaan Biosims

42 4Orofino Pharmaceuticals Group

43 5PAI Pharmaceutical Associates

44 4Pharmacore Inc

45 2Reach Pharmaceuticals

46 2Samson Medical Technologies

47 12Sandoz B2B

48 3Specpharm

49 2Spirig Healthcare

50 9Stragen Pharma SA

51 3Stravencon Limited

52 9Sun Pharmaceutical Industries Limited

53 1TECNOPHARMA Srl

54 3Teva Pharmaceutical Industries

55 1Theon Pharmaceuticals

56 3Umedica Laboratories

57 2Unosource Pharma

58 1Vaishali Pharma Ltd

59 3Viatris

60 3Villerton Invest Said

61 4World Medicine

62 6Zeiss Pharma

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PharmaCompass

01

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BioAsia
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

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BioAsia
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

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BioAsia
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

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BioAsia
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

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BioAsia
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

BioAsia
Not Confirmed
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BioAsia
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

BioAsia
Not Confirmed
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BioAsia
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

BioAsia
Not Confirmed
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BioAsia
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

BioAsia
Not Confirmed
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BioAsia
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

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10

BioAsia
Not Confirmed
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BioAsia
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

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11

BioAsia
Not Confirmed
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BioAsia
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

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12

BioAsia
Not Confirmed
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BioAsia
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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13

BioAsia
Not Confirmed
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BioAsia
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

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14

BioAsia
Not Confirmed
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BioAsia
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

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15

BioAsia
Not Confirmed
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BioAsia
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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16

BioAsia
Not Confirmed
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BioAsia
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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17

BioAsia
Not Confirmed
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BioAsia
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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18

BioAsia
Not Confirmed
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BioAsia
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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19

BioAsia
Not Confirmed
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BioAsia
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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20

BioAsia
Not Confirmed
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BioAsia
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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21

BioAsia
Not Confirmed
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BioAsia
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

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22

BioAsia
Not Confirmed
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BioAsia
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

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23

BioAsia
Not Confirmed
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BioAsia
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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24

BioAsia
Not Confirmed
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BioAsia
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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25

BioAsia
Not Confirmed
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BioAsia
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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26

BioAsia
Not Confirmed
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BioAsia
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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27

BioAsia
Not Confirmed
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BioAsia
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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28

BioAsia
Not Confirmed
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BioAsia
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

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29

BioAsia
Not Confirmed
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BioAsia
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

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30

BioAsia
Not Confirmed
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BioAsia
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

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