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01 3Aspen Pharmacare Holdings

02 1Strides Pharma Science

03 1Zeon Pharma Industries India Pvt Ltd

04 4ACS DOBFAR SPA

05 5ANI Pharmaceuticals Inc

06 1Antibiotice

07 1Apotex Inc

08 3Associated Biotech

09 5Aurobindo Pharma Limited

10 4Bausch Health

11 1Bernofarm Pharmaceutical Company

12 3Bio Labs

13 5Bristol Laboratories Ltd

14 7Bristol Myers Squibb

15 1Brix Biopharma

16 1CSPC Pharmaceutical Group

17 4Chartwell Pharmaceuticals llc

18 2DEVATS INDIA

19 1Ebb Medical

20 1Eloge

21 2Exeltis

22 1Generfarma Sl Laboratory

23 1Hainan Haiyao

24 4Hikma Pharmaceuticals

25 1IVAX Pharmaceuticals Inc

26 1Ideal Trade Links Uab

27 1JAMP PHARMA

28 4Jodas Expoim Pvt. Ltd

29 3Lupin Ltd

30 2MS Pharma

31 7Nectar Lifesciences

32 1PUREPAC PHARM

33 1Paranova Pharmaceuticals Ab

34 5Qualite Pharma

35 6Sandoz B2B

36 1Smith & Kenner Pharmaceuticals

37 5Sun Pharmaceutical Industries Limited

38 4Teva Pharmaceutical Industries

39 2Umedica Laboratories

40 3Viatris

41 6Warner Chilcott Company, LLC

42 1XL Laboratories Private Limited

43 1Xepa-Soul Pattinson m SDN BHD

44 5Zeiss Pharma

45 4Zim Laboratories

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PharmaCompass

01

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 BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

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

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothZeon Pharma is a manufacturer and supplier of APIs & Intermediates.

Regulatory Info :

Registration Country : India

Cefadroxil

Brand Name : Cefadroxil

Dosage Form : DC Granules

Dosage Strength :

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Zeon Pharma Industries India Pvt Ltd

04

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

05

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

06

IMCAS World Congress
Not Confirmed
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IMCAS World Congress
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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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07

IMCAS World Congress
Not Confirmed
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IMCAS World Congress
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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08

IMCAS World Congress
Not Confirmed
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IMCAS World Congress
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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09

IMCAS World Congress
Not Confirmed
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IMCAS World Congress
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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10

IMCAS World Congress
Not Confirmed
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IMCAS World Congress
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

IMCAS World Congress
Not Confirmed
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IMCAS World Congress
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

IMCAS World Congress
Not Confirmed
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IMCAS World Congress
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

IMCAS World Congress
Not Confirmed
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IMCAS World Congress
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

IMCAS World Congress
Not Confirmed
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IMCAS World Congress
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

IMCAS World Congress
Not Confirmed
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IMCAS World Congress
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

IMCAS World Congress
Not Confirmed
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IMCAS World Congress
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

IMCAS World Congress
Not Confirmed
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IMCAS World Congress
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

IMCAS World Congress
Not Confirmed
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IMCAS World Congress
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

blank

19

IMCAS World Congress
Not Confirmed
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IMCAS World Congress
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

blank

20

IMCAS World Congress
Not Confirmed
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IMCAS World Congress
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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