01 3Aspen Pharmacare Holdings
02 4ACS DOBFAR SPA
03 5ANI Pharmaceuticals Inc
04 1Antibiotice
05 1Apotex Inc
06 3Associated Biotech
07 5Aurobindo Pharma Limited
08 1Bausch Health
09 1Bernofarm Pharmaceutical Company
10 3Bio Labs
11 5Bristol Laboratories Ltd
12 7Bristol Myers Squibb
13 1Brix Biopharma
14 1CSPC Pharmaceutical Group
15 4Chartwell Pharmaceuticals llc
16 2DEVATS INDIA
17 1Ebb Medical
18 1Eloge
19 2Exeltis
20 1Generfarma Sl Laboratory
21 1Hainan Haiyao
22 4Hikma Pharmaceuticals
23 1IVAX Pharmaceuticals Inc
24 1JAMP PHARMA
25 4Jodas Expoim Pvt. Ltd
26 3Lupin Ltd
27 2MS Pharma
28 7Nectar Lifesciences
29 1PUREPAC PHARM
30 1Paranova Pharmaceuticals Ab
31 5Qualite Pharma
32 6Sandoz B2B
33 1Smith & Kenner Pharmaceuticals
34 1Strides Pharma SA (Pty) Ltd
35 5Sun Pharmaceutical Industries Limited
36 4Teva Pharmaceutical Industries
37 2Umedica Laboratories
38 3Viatris
39 6Warner Chilcott Company, LLC
40 1XL Laboratories Private Limited
41 1Xepa-Soul Pattinson m SDN BHD
42 5Zeiss Pharma
43 4Zim Laboratories
01 1CAP
02 11CAPSULE
03 14CAPSULE;ORAL
04 8Capsule
05 2Capsules
06 2DRY SUSPENSION
07 2DRY SYRUP
08 4Dispersible Tablet
09 2Dry Powder for Oral Suspension
10 2Dry Syrup
11 25FOR SUSPENSION;ORAL
12 2Film Coated Tablet
13 2Hard Capsule
14 4Oral Suspension
15 2Orodispersible Tablet
16 4Powder For Oral Suspension
17 2SUS
18 1SUSPENSION
19 2Suspensions
20 1TAB
21 3TABLET
22 7TABLET;ORAL
23 15Tablet
24 1Taste Masked Granules for Oral Suspension
25 1Uncoated Tablet
26 1capsules
01 5Approved
02 3Authorized
03 38DISCN
04 9Deregistered
05 22Generic
06 2Generic CTD, BE- Available
07 3Prescription
08 8RX
09 31Blank
01 1ALXIL
02 1APO-CEFADROXIL
03 3Bio-Oxil
04 34CEFADROXIL
05 1CEFORAN®
06 6Cefadroxil
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 37India
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
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 : ULTRACEF
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1GM BASE
Packaging :
Approval Date : 1982-08-31
Application Number : 62408
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 : CEFADROXIL
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1989-02-10
Application Number : 62695
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
