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01 3Aspen Pharmacare Holdings

02 1Strides Pharma Science

03 4ACS DOBFAR SPA

04 5ANI Pharmaceuticals Inc

05 1Apotex Inc

06 5Aurobindo Pharma Limited

07 1Bernofarm Pharmaceutical Company

08 3Bio Labs

09 5Bristol Laboratories Ltd

10 4Bristol Myers Squibb

11 1Brix Biopharma

12 1CSPC Pharmaceutical Group

13 4Chartwell Pharmaceuticals llc

14 2DEVATS INDIA

15 1Eloge

16 1Hainan Haiyao

17 4Hikma Pharmaceuticals

18 1IVAX Pharmaceuticals Inc

19 4Jodas Expoim Pvt. Ltd

20 3Lupin Ltd

21 2MS Pharma

22 7Nectar Lifesciences

23 1PUREPAC PHARM

24 1Pharma Swiss Ceska republika sro

25 2RANBAXY LABORATORIES LIMITED

26 1Sandoz B2B

27 1Smith & Kenner Pharmaceuticals

28 3Sun Pharmaceutical Industries Limited

29 4Teva Pharmaceutical Industries

30 2Umedica Laboratories

31 6Warner Chilcott Company, LLC

32 1XL Laboratories Private Limited

33 1Xepa-Soul Pattinson m SDN BHD

34 5Zeiss Pharma

35 4Zim Laboratories

36 2Blank

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PharmaCompass

01

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The Pharmacy Technology
Not Confirmed

Cefadroxil

Brand Name : Dacef

Dosage Form : CAP

Dosage Strength : 500mg

Packaging : 10X1mg

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info : Generic

Registration Country : South Africa

Cefadroxil Anhydrous

Brand Name : Cefadroxil 250 Strides

Dosage Form : TAB

Dosage Strength : 250mg

Packaging : 40X1mg

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Strides Pharma Science

03

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The Pharmacy Technology
Not Confirmed

Cefadroxil

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

Aspen API Comapny Banner

04

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The Pharmacy Technology
Not Confirmed

Cefadroxil

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

Aspen API Comapny Banner

05

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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

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06

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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

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07

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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

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08

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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

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09

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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

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10

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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

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11

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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

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12

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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

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13

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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

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14

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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

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15

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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

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16

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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

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17

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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

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18

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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

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19

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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

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20

The Pharmacy Technology
Not Confirmed
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The Pharmacy Technology
Not Confirmed

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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