01 1AbbVie Inc
02 1Towa Pharmaceutical
03 9ACS DOBFAR SPA
04 1ALMUS Srl
05 1ASTRO PHARMA VERTRIEB GMBH
06 3Acino Pharma (Pty) Ltd
07 2Actavis Inc
08 1Almus
09 2Ananta Medicare
10 2Antibiotice SA
11 6Aurobindo Pharma Limited
12 2B. Braun Medical
13 9Basil Pharmaceuticals
14 3Baxter Healthcare Corporation
15 3Bio Labs
16 2Biopharm
17 3C.T. LAB.FARMACEUTICO Srl
18 1CTSRL PHARMACEUTICAL LABORATORY
19 3DOC Generici
20 1EG SpA
21 4Eli Lilly
22 1Epifarma
23 2Esseti Farmaceutici
24 2F.I.R.M.A. SpA
25 1FG SRL
26 1FG Srl
27 2Firma
28 3Flagship Biotech International Pvt. Ltd
29 6Fresenius Kabi AB Brunna
30 3Fresenius Kabi Austria
31 3Fresenius SE & Co. KGaA
32 1GENETIC SpA
33 27GSK
34 2Hainan Haiyao
35 2Hanlim Pharmaceuticals Inc
36 1Health Biotech
37 6Hospira, Inc.
38 1IBN Savio
39 4Jodas Expoim Pvt. Ltd
40 2MIP Pharma
41 3Nectar Lifesciences
42 1NoroBio Pharmaceutical
43 2Oethmaan Biosims
44 1Orchid Pharma
45 10Orofino Pharmaceuticals Group
46 7PAI Pharmaceutical Associates
47 1Pensa Pharma
48 2Pfizer Inc
49 2S.F.GROUP Srl
50 2SF Group
51 6SIGMA TAU
52 4SO.SE.PHARM Srl
53 3STERIMAX INC
54 16Sandoz B2B
55 3Sekpharma
56 1So.Se.Pharm
57 9Stragen Pharma SA
58 1Theon Pharmaceuticals
59 2Viatris
60 3Villerton Invest Said
61 1Wockhardt
62 3World Medicine
63 2Xiangbei Welman Pharmaceuticals
64 2Yangtze River Pharmaceutical Group
65 2Zeiss Pharma
66 2Blank
01 21Ceftazidima 1.000Mg 1 Unit Parenteral Use
02 6Ceftazidima 1.000Mg 1 Unit Parenteral Use Ev
03 1Ceftazidima 1.000Mg 10 Units Parenteral Use Im Ev
04 6Ceftazidima 2.000Mg 1 Unit Parenteral Use Ev
05 2Ceftazidima 250Mg 1 Unit Parenteral Use
06 4Ceftazidima 500Mg 1 Unit Parenteral Use
07 4Dry Sub
08 15INJ
09 3INJECTABLE
10 41INJECTABLE;INJECTION
11 5INJECTION
12 31Injection
13 1POI
14 2POWDER FOR INJECTION / INFUSION
15 6POWDER FOR SOLUTION
16 5POWDER FOR SOLUTION FOR INFUSION
17 7POWDER FOR SOLUTION FOR INJECTION
18 1POWDER;INTRAVENOUS
19 15Powder And Solvent For Injection
20 2Powder And Solvent For Solution
21 14Powder for Injection
22 6Powder for Solution for Injection / Infusion
23 2Powder for injection
24 6Powder for injection fluid, resolution
25 8Powder for injection/infusion fluid, resolution
26 1Powder+1 Vial Solv.3Ml
27 3VIAL
28 1Vial
29 2powder for injection/Infusion
01 33DISCN
02 30Generic
03 4Originator
04 6Prescription
05 9RX
06 139Blank
01 1AVYCAZ
02 3Biozid
03 2CEFTAMIL®
04 9CEFTAZIDIME
05 1CEFTAZIDIME ALMUS
06 1CEFTAZIDIME ASTRO-PHARMA
07 1CEFTAZIDIME DOC
08 1CEFTAZIDIME EG STADA
09 3CEFTAZIDIME FOR INJECTION BP
10 3CEFTAZIDIME FOR INJECTION, USP
11 2CEFTAZIDIME IN DEXTROSE CONTAINER
12 1CEFTAZIDIME KABI
13 1CEFTAZIDIME MYLAN GENERICS
14 1CEFTAZIDIME SANDOZ
15 3CEFTAZIDIME SODIUM IN PLASTIC CONTAINER
16 1CEFTAZIDIME THINK
17 4CEPTAZ
18 11Ceftazida
19 3Ceftazidim Fresenius Kabi
20 2Ceftazidim MIP
21 3Ceftazidim Stragen
22 3Ceftazidim Villerton
23 3Ceftazidima
24 2Ceftazidime 1g Oethmaan
25 1Ceftazidime Normon 1G 1V+Amp Polv+Dis Sol Inj Efg
26 1DELTAZIME
27 1Deltaze
28 2Deltazime
29 1Dizatec
30 1ETAZIM
31 3Ectrum
32 1Etaz
33 4FORTAZ
34 3FORTAZ IN PLASTIC CONTAINER
35 1FRIBAT
36 3Fortam
37 1Fortam 1G/Vial 1 Injection
38 13Fortum
39 1Fresenius Ceftazidime 1 000 mg
40 1Fresenius Ceftazidime 2 000 mg
41 2GLAZIDIM
42 2Glazid
43 1Glazid
44 1Glazidim
45 1Glazidim Monovial 2
46 1Glazidim Vein 1
47 1Glazidim Vein 2
48 1HANLIM CEFMETAZOLE SODIUM
49 1HANLIM CEFTAZIDIME SODIUM
50 1Keftaz 0.5G
51 1Keftaz 1,0G
52 1Keftaz 1,0g
53 1Keftaz 2,0G
54 1LIOTIXIL
55 1Liotixil
56 1Orzid 2 g
57 6PENTACEF
58 1Panzid
59 2STARCEF
60 2Spectrum
61 2Starcef
62 6TAZICEF
63 1TAZIDIF
64 2TAZIDIME
65 2TAZIDIME IN PLASTIC CONTAINER
66 1THEOZIDE-500
67 1TOTTIZIM
68 1Tazidif
69 1Taziject 0,5 G
70 1Taziject 1,0 G
71 1Taziject 2,0 G
72 2Tottiz
73 2Tottizim
74 2Zavicefta
75 2ceftazidime Actavis
76 5ceftazidime Sandoz
77 57Blank
01 6Canada
02 7China
03 25India
04 73Italy
05 14Norway
06 3Pakistan
07 2Romania
08 16South Africa
09 2South Korea
10 2Spain
11 14Sweden
12 4Switzerland
13 3Turkey
14 42USA
15 2United Kingdom
16 6Blank
Regulatory Info : RX
Registration Country : USA
Brand Name : AVYCAZ
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : EQ 0.5GM BASE;2GM/VIAL
Packaging :
Approval Date : 2015-02-25
Application Number : 206494
Regulatory Info : RX
Registration Country : USA
Towa Pharma is dedicated to researching, developing, producing, and promoting generic drugs.
Regulatory Info :
Registration Country : Italy
Brand Name : CEFTAZIDIME THINK
Dosage Form : Powder And Solvent For Injection
Dosage Strength : 1 g/3 ml
Packaging : 1 UNIT 1000 MG - PARENTERAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFTAZIDIME
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 500MG/VIAL
Packaging :
Approval Date : 1985-11-20
Application Number : 62640
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CEFTAZIDIME
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1GM/VIAL
Packaging :
Approval Date : 1985-11-20
Application Number : 62640
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CEFTAZIDIME
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2GM/VIAL
Packaging :
Approval Date : 1985-11-20
Application Number : 62640
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CEFTAZIDIME
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 6GM/VIAL
Packaging :
Approval Date : 1992-02-03
Application Number : 62640
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFTAZIDIME IN DEXTROSE CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE
Packaging :
Approval Date : 2011-06-13
Application Number : 50823
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFTAZIDIME IN DEXTROSE CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE
Packaging :
Approval Date : 2011-06-13
Application Number : 50823
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFTAZIDIME SODIUM IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG BASE/ML
Packaging :
Approval Date : 1993-04-29
Application Number : 63221
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFTAZIDIME SODIUM IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/ML
Packaging :
Approval Date : 1993-04-29
Application Number : 63221
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFTAZIDIME SODIUM IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 40MG BASE/ML
Packaging :
Approval Date : 1993-04-29
Application Number : 63221
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TAZIDIME
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1GM/VIAL
Packaging :
Approval Date : 1985-11-20
Application Number : 62655
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TAZIDIME
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2GM/VIAL
Packaging :
Approval Date : 1985-11-20
Application Number : 62655
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TAZIDIME IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1GM/VIAL
Packaging :
Approval Date : 1986-07-10
Application Number : 62739
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TAZIDIME IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2GM/VIAL
Packaging :
Approval Date : 1986-07-10
Application Number : 62739
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEPTAZ
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 500MG/VIAL
Packaging :
Approval Date : 1990-09-27
Application Number : 50646
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEPTAZ
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1GM/VIAL
Packaging :
Approval Date : 1990-09-27
Application Number : 50646
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEPTAZ
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2GM/VIAL
Packaging :
Approval Date : 1990-09-27
Application Number : 50646
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEPTAZ
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10GM/VIAL
Packaging :
Approval Date : 1990-09-27
Application Number : 50646
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TAZICEF
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 500MG/VIAL
Packaging :
Approval Date : 1986-03-06
Application Number : 62662
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TAZICEF
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1GM/VIAL
Packaging :
Approval Date : 1986-03-06
Application Number : 62662
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TAZICEF
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2GM/VIAL
Packaging :
Approval Date : 1986-03-06
Application Number : 62662
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TAZICEF
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 6GM/VIAL
Packaging :
Approval Date : 1986-03-06
Application Number : 62662
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FORTAZ
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1985-07-19
Application Number : 50578
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FORTAZ
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1985-07-19
Application Number : 50578
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FORTAZ
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1985-07-19
Application Number : 50578
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FORTAZ
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 6GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1985-07-19
Application Number : 50578
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FORTAZ IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG BASE/ML
Packaging :
Approval Date : 1989-04-28
Application Number : 50634
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FORTAZ IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/ML
Packaging :
Approval Date : 1989-04-28
Application Number : 50634
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FORTAZ IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 40MG BASE/ML
Packaging :
Approval Date : 1989-04-28
Application Number : 50634
Regulatory Info : DISCN
Registration Country : USA
LOOKING FOR A SUPPLIER?
