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01 5ANI PHARMS

02 4APOTHECON

03 2AUROBINDO

04 1AUROBINDO PHARMA

05 5BRISTOL

06 4CHARTWELL RX

07 1CSPC OUYI

08 2HIKMA

09 2HIKMA PHARMS

10 1IVAX SUB TEVA PHARMS

11 3LUPIN

12 1PUREPAC PHARM

13 1RANBAXY

14 1RANBAXY LABS LTD

15 1SANDOZ

16 3SUN PHARM INDS LTD

17 1TEVA

18 2TEVA PHARMS

19 6WARNER CHILCOTT

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PharmaCompass

01

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Brand Name : CEFADROXIL

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 125MG BASE/5ML

Approval Date : 1982-01-01

Application Number : 62334

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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02

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Brand Name : CEFADROXIL

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 250MG BASE/5ML

Approval Date : 1982-01-01

Application Number : 62334

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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03

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Brand Name : CEFADROXIL

Dosage Form : FOR SUSPENSION;ORAL

Dosage Strength : EQ 500MG BASE/5ML

Approval Date : 1982-01-01

Application Number : 62334

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

Fi Europe 2024
Not Confirmed
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05

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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Dosage Strength : EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 50512

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Brand Name : DURICEF

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 250MG BASE

Approval Date : 1982-01-01

Application Number : 50512

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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07

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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**

Approval Date : 1982-01-01

Application Number : 50527

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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**

Approval Date : 1982-01-01

Application Number : 50527

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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**

Approval Date : 1982-01-01

Application Number : 50527

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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10

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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**

Approval Date : 1982-01-01

Application Number : 50528

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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