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 1Bernofarm Pharmaceutical Company
09 3Bio Labs
10 5Bristol Laboratories Ltd
11 4Bristol Myers Squibb
12 1Brix Biopharma
13 1CSPC Pharmaceutical Group
14 4Chartwell Pharmaceuticals llc
15 2DEVATS INDIA
16 1Eloge
17 1Hainan Haiyao
18 4Hikma Pharmaceuticals
19 1IVAX Pharmaceuticals Inc
20 1JAMP PHARMA
21 4Jodas Expoim Pvt. Ltd
22 3Lupin Ltd
23 2MS Pharma
24 7Nectar Lifesciences
25 1PUREPAC PHARM
26 1Pharma Swiss Ceska republika sro
27 5Qualite Pharma
28 4Sandoz B2B
29 1Smith & Kenner Pharmaceuticals
30 1Strides Pharma SA (Pty) Ltd
31 5Sun Pharmaceutical Industries Limited
32 4Teva Pharmaceutical Industries
33 2Umedica Laboratories
34 3Viatris
35 6Warner Chilcott Company, LLC
36 1XL Laboratories Private Limited
37 1Xepa-Soul Pattinson m SDN BHD
38 5Zeiss Pharma
39 4Zim Laboratories
40 2Blank
01 1CAP
02 11CAPSULE
03 14CAPSULE;ORAL
04 7Capsule
05 2Capsules
06 2DRY SUSPENSION
07 2DRY SYRUP
08 4Dispersible Tablet
09 2Dry Powder for Oral Suspension
10 2Dry Syrup
11 2FILM COATED PILL
12 25FOR SUSPENSION;ORAL
13 2HARD CAPSULES
14 4Oral Suspension
15 2POWDER FOR ORAL SUSPENSION
16 1SOLUBLE TABLET
17 2SUS
18 1SUSPENSION
19 2Suspensions
20 1TAB
21 3TABLET
22 7TABLET;ORAL
23 11Tablet
24 1Taste Masked Granules for Oral Suspension
25 1Uncoated Tablet
26 1capsules
01 38DISCN
02 22Generic
03 2Generic CTD, BE- Available
04 8RX
05 43Blank
01 1ALXIL
02 1APO-CEFADROXIL
03 3Bio-Oxil
04 34CEFADROXIL
05 1CEFORAN®
06 6Cefadroxil
07 1Cefadroxil 250 Strides
08 2Cefadroxil ; Potassium Clavulanate
09 1Cefadroxil J. And A. Sabater 500Mg 28 Capsules
10 3Cefadroxil Sandoz
11 1Cefamox soluble
12 6DURICEF
13 1Dacef
14 1Dacef Suspension 250 Mg/5 Ml
15 1Dacef Suspension 500 Mg/5 Mg
16 1Duracef 500Mg 28 Capsules
17 1Franroxil
18 1JAMP CEFADROXIL
19 1Sofidrox
20 1TEVA-CEFADROXIL
21 2UFEROXIL
22 6ULTRACEF
23 1WINCOCEF
24 3cefadroxil
25 33Blank
01 1Cambodia
02 3Canada
03 1China
04 37India
05 4Italy
06 2Jordan
07 1Malaysia
08 3Pakistan
09 1Romania
10 4South Africa
11 2Spain
12 7Sweden
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
