Visitor Monitoring Drug Details: DURICEF
 
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Drug Details

Drug Name: DURICEF
FDA Application No: (NDA) 050512
Active Ingredient(s): CEFADROXIL/CEFADROXIL HEMIHYDRATE
Company: WARNER CHILCOTT
Original Approval or Tentative Approval Date: February 17, 1978
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
DURICEF CEFADROXIL/CEFADROXIL HEMIHYDRATEEQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**CAPSULE; ORAL Discontinued No None
DURICEF CEFADROXIL/CEFADROXIL HEMIHYDRATEEQ 250MG BASECAPSULE; ORAL Discontinued No None


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