01 3Aspen Pharmacare Holdings
02 4ACS DOBFAR SPA
03 5ANI Pharmaceuticals Inc
04 1Apotex Inc
05 5Aurobindo Pharma Limited
06 1Bernofarm Pharmaceutical Company
07 3Bio Labs
08 5Bristol Laboratories Ltd
09 4Bristol Myers Squibb
10 1Brix Biopharma
11 1CSPC Pharmaceutical Group
12 4Chartwell Pharmaceuticals llc
13 1Cipla Medpro South Africa
14 2DEVATS INDIA
15 1Eloge
16 1Hainan Haiyao
17 4Hikma Pharmaceuticals
18 1IVAX Pharmaceuticals Inc
19 1JAMP PHARMA
20 4Jodas Expoim Pvt. Ltd
21 3Lupin Ltd
22 2MS Pharma
23 7Nectar Lifesciences
24 1PUREPAC PHARM
25 1Pharma Swiss Ceska republika sro
26 2RANBAXY LABORATORIES LIMITED
27 1Sandoz B2B
28 1Smith & Kenner Pharmaceuticals
29 3Sun Pharmaceutical Industries Limited
30 4Teva Pharmaceutical Industries
31 2Umedica Laboratories
32 6Warner Chilcott Company, LLC
33 1XL Laboratories Private Limited
34 1Xepa-Soul Pattinson m SDN BHD
35 5Zeiss Pharma
36 4Zim Laboratories
37 2Blank
01 1CAP
02 11CAPSULE
03 14CAPSULE;ORAL
04 6Capsule
05 2Capsules
06 2DRY SUSPENSION
07 2DRY SYRUP
08 4Dispersible Tablet
09 2Dry Powder for Oral Suspension
10 1Dry Syrup
11 25FOR SUSPENSION;ORAL
12 4Oral Suspension
13 1SOLUBLE TABLET
14 2SUS
15 1SUSPENSION
16 2Suspensions
17 1TAB
18 3TABLET
19 7TABLET;ORAL
20 5Tablet
21 1Taste Masked Granules for Oral Suspension
22 1Uncoated Tablet
01 38DISCN
02 22Generic
03 2Generic CTD, BE- Available
04 8RX
05 28Blank
01 1ALXIL
02 1APO-CEFADROXIL
03 3Bio-Oxil
04 34CEFADROXIL
05 1Cefadroxil J. And A. Sabater 500Mg 28 Capsules
06 1Cefamox soluble
07 1Cipadur 250Mg Dt
08 6DURICEF
09 1Dacef
10 1Dacef Suspension 250 Mg/5 Ml
11 1Dacef Suspension 500 Mg/5 Mg
12 1Duracef 500Mg 28 Capsules
13 1Franroxil
14 1JAMP CEFADROXIL
15 1Sofidrox
16 1TEVA-CEFADROXIL
17 2UFEROXIL
18 6ULTRACEF
19 1WINCOCEF
20 33Blank
01 1Cambodia
02 3Canada
03 1China
04 29India
05 4Italy
06 2Jordan
07 1Malaysia
08 3Pakistan
09 4South Africa
10 2Spain
11 1Sweden
12 46USA
13 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 : CEFADROXIL
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 125MG BASE/5ML
Packaging :
Approval Date : 1989-03-01
Application Number : 62698
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 : 1989-03-01
Application Number : 62698
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 : 1989-03-01
Application Number : 62698
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 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 : 1987-03-03
Application Number : 62766
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 : 1989-01-05
Application Number : 63017
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 : 1999-06-22
Application Number : 65015
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : CEFADROXIL
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1GM BASE
Packaging :
Approval Date : 1999-04-23
Application Number : 65018
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 : FOR SUSPENSION;ORAL
Dosage Strength : EQ 125MG BASE/5ML
Packaging :
Approval Date : 2003-03-26
Application Number : 65115
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 : 2003-03-26
Application Number : 65115
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 : RX
Registration Country : USA
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : CEFADROXIL
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1GM BASE
Packaging :
Approval Date : 1987-04-08
Application Number : 62774
Regulatory Info : RX
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
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