01 3Aspen Pharmacare Holdings
02 1Strides Pharma Science
03 1Zeon Pharma Industries India Pvt Ltd
04 4ACS DOBFAR SPA
05 5ANI Pharmaceuticals Inc
06 1Antibiotice
07 1Apotex Inc
08 3Associated Biotech
09 5Aurobindo Pharma Limited
10 1Bausch Health
11 1Bernofarm Pharmaceutical Company
12 3Bio Labs
13 5Bristol Laboratories Ltd
14 7Bristol Myers Squibb
15 1Brix Biopharma
16 1CSPC Pharmaceutical Group
17 4Chartwell Pharmaceuticals llc
18 2DEVATS INDIA
19 1Ebb Medical
20 1Eloge
21 2Exeltis
22 1Generfarma Sl Laboratory
23 1Hainan Haiyao
24 4Hikma Pharmaceuticals
25 1IVAX Pharmaceuticals Inc
26 1JAMP PHARMA
27 4Jodas Expoim Pvt. Ltd
28 3Lupin Ltd
29 2MS Pharma
30 7Nectar Lifesciences
31 1PUREPAC PHARM
32 1Paranova Pharmaceuticals Ab
33 5Qualite Pharma
34 6Sandoz B2B
35 1Smith & Kenner Pharmaceuticals
36 5Sun Pharmaceutical Industries Limited
37 4Teva Pharmaceutical Industries
38 2Umedica Laboratories
39 3Viatris
40 6Warner Chilcott Company, LLC
41 1XL Laboratories Private Limited
42 1Xepa-Soul Pattinson m SDN BHD
43 5Zeiss Pharma
44 4Zim Laboratories
01 1CAP
02 11CAPSULE
03 14CAPSULE;ORAL
04 8Capsule
05 2Capsules
06 1DC Granules
07 2DRY SUSPENSION
08 2DRY SYRUP
09 4Dispersible Tablet
10 2Dry Powder for Oral Suspension
11 2Dry Syrup
12 25FOR SUSPENSION;ORAL
13 2Film Coated Tablet
14 2Hard Capsule
15 4Oral Suspension
16 2Orodispersible Tablet
17 4Powder For Oral Suspension
18 2SUS
19 1SUSPENSION
20 2Suspensions
21 1TAB
22 3TABLET
23 7TABLET;ORAL
24 15Tablet
25 1Taste Masked Granules for Oral Suspension
26 1Uncoated Tablet
27 1capsules
01 5Approved
02 3Authorized
03 38DISCN
04 9Deregistered
05 22Generic
06 2Generic CTD, BE- Available
07 3Prescription
08 8RX
09 32Blank
01 1ALXIL
02 1APO-CEFADROXIL
03 3Bio-Oxil
04 34CEFADROXIL
05 1CEFORAN®
06 7Cefadroxil
07 1Cefadroxil 250 Strides
08 2Cefadroxil ; Potassium Clavulanate
09 1Cefadroxil Mylan
10 3Cefadroxil Sandoz
11 2Cefadroxil Viatris
12 1Cefadroxilo Desgen
13 4Cefamox
14 2Cefamox L?slig
15 2Cinfexil
16 6DURICEF
17 1Dacef
18 1Dacef Suspension 250 Mg/5 Ml
19 1Dacef Suspension 500 Mg/5 Mg
20 2Duracef
21 1Franroxil
22 1JAMP CEFADROXIL
23 1Sofidrox
24 1TEVA-CEFADROXIL
25 2UFEROXIL
26 6ULTRACEF
27 1WINCOCEF
28 33Blank
01 1Cambodia
02 3Canada
03 1China
04 38India
05 4Italy
06 2Jordan
07 1Malaysia
08 3Pakistan
09 1Romania
10 4South Africa
11 3Spain
12 14Sweden
13 46USA
14 1Vietnam
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Dacef
Dosage Form : CAP
Dosage Strength : 500mg
Packaging : 10X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Synergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Cefadroxil 250 Strides
Dosage Form : TAB
Dosage Strength : 250mg
Packaging : 40X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Zeon Pharma is a manufacturer and supplier of APIs & Intermediates.
Regulatory Info :
Registration Country : India
Brand Name : Cefadroxil
Dosage Form : DC Granules
Dosage Strength :
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Dacef Suspension 250 Mg/5 Ml
Dosage Form : SUS
Dosage Strength : 250mg/5ml
Packaging : 60X1mg/5ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Dacef Suspension 500 Mg/5 Mg
Dosage Form : SUS
Dosage Strength : 500mg/5ml
Packaging : 60X1mg/5ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : ULTRACEF
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 125MG BASE/5ML
Packaging :
Approval Date : 1982-03-16
Application Number : 62376
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : ULTRACEF
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 250MG BASE/5ML
Packaging :
Approval Date : 1982-03-16
Application Number : 62376
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : ULTRACEF
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 500MG BASE/5ML
Packaging :
Approval Date : 1982-03-16
Application Number : 62376
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : ULTRACEF
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1982-03-16
Application Number : 62378
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : CEFADROXIL
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 125MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62334
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : CEFADROXIL
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 250MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62334
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : CEFADROXIL
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 500MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62334
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : ULTRACEF
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1GM BASE
Packaging :
Approval Date : 1982-06-10
Application Number : 62390
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : CEFADROXIL
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 62291
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : DURICEF
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50512
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : DURICEF
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 50512
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : DURICEF
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 500MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50527
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : DURICEF
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50527
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : DURICEF
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50527
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : DURICEF
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1GM BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50528
Regulatory Info : DISCN
Registration Country : USA
