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Duricef (Cefadroxil)
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Buy Duricef (Cefadroxil)

What is Duricef? Duricef (Cefadroxil) is a cephalosporin antibiotic used to treat certain infections caused by bacteria such as skin, throat, and urinary tract infections. Duricef (Cefadroxil) may also be used to treat other conditions as determined by your doctor. Click for more Duricef details.


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Also known as: Baxan, Bidocef, Cefadril, Cefadroxilum, Cefadur, Cephadroxil, Cepotec, Duracef, Oradroxil, Orelox, Parahydroxycefalexine, Podomexef, Teroxina, Ultracef, Cefadroxil (generic name).
In Mexico: Cefadroxilo.

A brand of Duricef labelled as Cefadur is at Freedom Pharmacy

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MedicationStrengthQuantityPriceFreedom Pharmacy
Cefadur500 mg100 capsules capsules$107.79Order


A brand of Duricef labelled as Cefadroxil made by 1 A Pharma and Hexal, Cefadroxilo by Generfarma Sl, Orelox manufactured by Daiichi Sankyo Deutschland, and Podomexef made by Daiichi Sankyo Deutschland are at Goldpharma

MedicationStrengthQuantityPriceGoldpharma
Cefadroxil250 mg60ml suspension$24.30Order
Cefadroxil500 mg10 tablets$28.98Order
Cefadroxil500 mg20 tablets$38.96Order
Cefadroxil1000 mg10 tablets$38.96Order
Cefadroxil1000 mg20 tablets$74.19Order
Cefadroxil Forte500 mg60ml suspension$30.55Order
Cefadroxilo500 mg28 capsules$21.09Order
Orelox100 mg20 tablets$45.58Order
Orelox200 mg15 tablets$56.73Order
Podomexef100 mg10 tablets$35.02Order
Podomexef100 mg30 tablets$56.73Order
Podomexef200 mg10 tablets$45.58Order
Podomexef Saft40 mg50ml suspension$27.48Order



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Duricef - HealthCare News

Approval Expanded for Sapien Artificial Heart Valve

MONDAY, Oct. 22 (HealthDay News) -- U.S. Food and Drug Administration approval for the Sapien Transcatheter Heart Valve has been expanded to include additional people with aortic valve stenosis, the medical term for a narrowing of the aortic valve that prevents the valve from functioning properly.

The new approval sanctions the artificial valve for patients who are at above-average risk of complications from valve surgery, including the possibility of death, the agency said Friday in a news release. The valve was first approved in 2011.

Read entire article...

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