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01 3Aspen Pharmacare Holdings

02 4ACS DOBFAR SPA

03 5ANI Pharmaceuticals Inc

04 1Antibiotice SA

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

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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

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

03

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

04

Discovery Europe
Not Confirmed
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Discovery Europe
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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05

Discovery Europe
Not Confirmed
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Discovery Europe
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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06

Discovery Europe
Not Confirmed
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Discovery Europe
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

blank

07

Discovery Europe
Not Confirmed
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Discovery Europe
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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08

Discovery Europe
Not Confirmed
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Discovery Europe
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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09

Discovery Europe
Not Confirmed
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Discovery Europe
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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10

Discovery Europe
Not Confirmed
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Discovery Europe
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

blank

11

Discovery Europe
Not Confirmed
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Discovery Europe
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

blank

12

Discovery Europe
Not Confirmed
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Discovery Europe
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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13

Discovery Europe
Not Confirmed
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Discovery Europe
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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14

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

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

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15

Discovery Europe
Not Confirmed
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Discovery Europe
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

Discovery Europe
Not Confirmed
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Discovery Europe
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

blank

17

Discovery Europe
Not Confirmed
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Discovery Europe
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

Discovery Europe
Not Confirmed
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Discovery Europe
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

Discovery Europe
Not Confirmed
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Discovery Europe
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

Discovery Europe
Not Confirmed
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Discovery Europe
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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