01 3Aspen Pharmacare Holdings
02 1Strides Pharma Science
03 4ACS DOBFAR SPA
04 5ANI Pharmaceuticals Inc
05 1Antibiotice SA
06 1Apotex Inc
07 3Associated Biotech
08 5Aurobindo Pharma Limited
09 1Bernofarm Pharmaceutical Company
10 3Bio Labs
11 5Bristol Laboratories Ltd
12 4Bristol Myers Squibb
13 1Brix Biopharma
14 1CSPC Pharmaceutical Group
15 4Chartwell Pharmaceuticals llc
16 2DEVATS INDIA
17 1Eloge
18 1Hainan Haiyao
19 4Hikma Pharmaceuticals
20 1IVAX Pharmaceuticals Inc
21 1JAMP PHARMA
22 4Jodas Expoim Pvt. Ltd
23 3Lupin Ltd
24 2MS Pharma
25 7Nectar Lifesciences
26 1PUREPAC PHARM
27 1Pharma Swiss Ceska republika sro
28 4Sandoz B2B
29 1Smith & Kenner Pharmaceuticals
30 5Sun Pharmaceutical Industries Limited
31 4Teva Pharmaceutical Industries
32 2Umedica Laboratories
33 3Viatris
34 6Warner Chilcott Company, LLC
35 1XL Laboratories Private Limited
36 1Xepa-Soul Pattinson m SDN BHD
37 5Zeiss Pharma
38 4Zim Laboratories
39 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 6Tablet
24 1Taste Masked Granules for Oral Suspension
25 1Uncoated Tablet
26 1capsules
01 38DISCN
02 22Generic
03 2Generic CTD, BE- Available
04 3Prescription
05 8RX
06 35Blank
01 1ALXIL
02 1APO-CEFADROXIL
03 3Bio-Oxil
04 34CEFADROXIL
05 1CEFORAN®
06 3Cefadroxil
07 1Cefadroxil 250 Strides
08 1Cefadroxil J. And A. Sabater 500Mg 28 Capsules
09 3Cefadroxil Sandoz
10 1Cefamox soluble
11 6DURICEF
12 1Dacef
13 1Dacef Suspension 250 Mg/5 Ml
14 1Dacef Suspension 500 Mg/5 Mg
15 1Duracef 500Mg 28 Capsules
16 1Franroxil
17 1JAMP CEFADROXIL
18 1Sofidrox
19 1TEVA-CEFADROXIL
20 2UFEROXIL
21 6ULTRACEF
22 1WINCOCEF
23 3cefadroxil
24 33Blank
01 1Cambodia
02 3Canada
03 1China
04 32India
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
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
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
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 : 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
