01 5Aspen Pharmacare Holdings
02 10ACS DOBFAR SPA
03 5Actavis Inc
04 6Adcock Ingram
05 2Akriti Pharmaceuticals Pvt. Ltd.
06 2Antibiotice SA
07 4Ascend Labs
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 15GSK
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 9RANBAXY LABORATORIES LIMITED
46 2Reach Pharmaceuticals
47 2Samson Medical Technologies
48 18Sandoz B2B
49 3Specpharm
50 2Spirig Healthcare
51 9Stragen Pharma SA
52 3Stravencon 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
01 2Cefuroxime 1.000Mg 1 Unit Parenteral Use
02 1Cefuroxime 250Mg/5Ml 50Ml Oral Use
03 1Cefuroxime 500Mg 2Ml 1 Units Parenteral Use
04 1Dry Powder for Oral Suspension
05 2Dry Sub
06 2FCT
07 2Film-Coated Tablets
08 8Filmtabl
09 18INJ
10 3INJECTABLE
11 24INJECTABLE;INJECTION
12 9INJECTABLE;INTRAMUSCULAR, INTRAVENOUS
13 2INJECTABLE;INTRAVENOUS
14 4INJECTION
15 1Injectables
16 24Injection
17 3Oral Suspension
18 2POI
19 2POWDER AND SOLVENT FOR SOLUTION FOR INFUSION
20 4POWDER FOR INJECTION
21 11POWDER FOR INJECTION / INFUSION
22 2POWDER FOR SOLUTION
23 3POWDER FOR SOLUTION FOR INFUSION
24 9POWDER FOR SOLUTION FOR INJECTION
25 3Powder for IM/IV Injection
26 9Powder for Injection
27 3Powder for Solution for Injection / Infusion
28 3Powder for injection fluid, resolution
29 2Powder for injection fluid, suspension or resolution
30 4Powder for injection/infusion fluid
31 6Powder for injection/infusion fluid, resolution
32 8SUS
33 1Susp
34 22TAB
35 2powder for injection/Infusion
36 2tablet
37 9Blank
01 31DISCN
02 62Generic
03 8Originator
04 2Prescription
05 4RX
06 107Blank
01 2Adco Cefuroxime 1.5g (20ml)
02 2Adco-Cefuroxime 250 mg
03 2Adco-Cefuroxime 750mg
04 3Aksef
05 1Alkoxime 250 mg
06 1Alkoxime 500 mg
07 2Aprokam
08 1Aspen Cefuroxime 1,5 G
09 1Aspen Cefuroxime 250 Mg
10 1Aspen Cefuroxime 750 Mg
11 2Betaroxime
12 2CEFUROXIME AND DEXTROSE IN DUPLEX CONTAINER
13 2CEFUROXIME Atb®
14 2CEFUROXIME FOR INJECTION, USP
15 19CEFUROXIME SODIUM
16 2CEFUROXIME SODIUM IN PLASTIC CONTAINER
17 1Cefasyn 250
18 1Cefasyn 500
19 1Cefasyn-250
20 1Cefasyn-500
21 1Cefu-Hexal 250
22 1Cefu-Hexal 500
23 2Cefuroxim Axapharm
24 2Cefuroxim Fresenius Kabi
25 2Cefuroxim MIP
26 2Cefuroxim Sandoz
27 2Cefuroxim Spirig HC
28 3Cefuroxim Stragen
29 3Cefuroxim Villerton
30 2Cefuroxim-Mepha
31 1Cefuroxime 125mg/5ml Oethmaan
32 1Cefuroxime 250 Oethmaan
33 1Cefuroxime 500 Oethmaan
34 2Cefuroxime B. Braun
35 2Cefuroxime Kabi
36 2Cefuroxime MIP
37 3Cefuroxime Mylan
38 3Cefuroxime Stravencon
39 3Cefuroxime Want Fullerton
40 1Ceroxim 500 Tablets
41 2Ceroxim Forte Suspension
42 1Ceroxim 250 Tablets
43 2Ceroxim Suspension
44 2Curox
45 1Curoxim Vein 1
46 1Curoxim Vein 2
47 1FKSA Cefuroxime 1 500 mg
48 1FKSA Cefuroxime 750 mg
49 2Furocsem
50 1Gulf Cefuroxime 750
51 1HANLIM CEFUROXIME SODIUM
52 1Itorex
53 5KEFUROX
54 2KEFUROX IN PLASTIC CONTAINER
55 1Lafurex
56 1Medaxime 1,5
57 1Medaxime 250
58 1Medaxime 750
59 1Orax
60 1Orchid Cefuroxime 250 mg
61 1Orchid Cefuroxime 500 mg
62 4Pharmacor Cefuroxime
63 2SIRUMEK
64 1Sandoz Cefuroxime
65 1Sandoz-Cefuroxime 125mg/5ml
66 1Sinoxim
67 1THEOROXIME-250nDry Syrup
68 3UROXIME
69 3ZINACEF
70 2ZINACEF IN PLASTIC CONTAINER
71 1Zefroxe 250 Tablets
72 1Zefroxe 500 Tablets
73 10Zinacef
74 2Zinacef (Monovial)
75 1Zinacef 1,5 g Injection
76 1Zinacef 250 mg Injection
77 1Zinacef 750 mg Injection
78 3Zinat
79 2Zinnat
80 2Zinnat (UK)
81 2Zinnat Suspension 125 mg
82 1Zinnat Tablets 125mg
83 1Zinnat Tablets 250mg
84 1Zinnat Tablets 500mg
85 1Zinuroz 250
86 1Zinuroz 500
87 3cefuroxime Stragen
88 44Blank
01 8Australia
02 2Canada
03 4China
04 29India
05 15Italy
06 15Norway
07 2Romania
08 52South Africa
09 1South Korea
10 25Sweden
11 13Switzerland
12 10Turkey
13 35USA
14 3Blank
Regulatory Info : Generic
Registration Country : South Africa
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
Regulatory Info : Generic
Registration Country : South Africa
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
Regulatory Info : Generic
Registration Country : South Africa
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
Regulatory Info :
Registration Country : Australia
Brand Name : Zinnat
Dosage Form :
Dosage Strength :
Packaging : 20
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Zinnat
Dosage Form :
Dosage Strength :
Packaging : 20
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ZINACEF
Dosage Form : INJECTABLE;INTRAMUSCULAR, INTRAVENOUS
Dosage Strength : EQ 750MG BASE/VIAL
Packaging :
Approval Date : 1983-10-19
Application Number : 50558
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ZINACEF
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1.5GM BASE/VIAL
Packaging :
Approval Date : 1983-10-19
Application Number : 50558
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ZINACEF
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 7.5GM BASE/VIAL
Packaging :
Approval Date : 1986-10-23
Application Number : 50558
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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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