Visitor Monitoring Drug Details: DURICEF
 
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Drug Details

Drug Name: DURICEF
FDA Application No: (NDA) 050527
Active Ingredient(s): CEFADROXIL/CEFADROXIL HEMIHYDRATE
Company: WARNER CHILCOTT
Original Approval or Tentative Approval Date: September 12, 1980
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
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/5MLFOR SUSPENSION; ORAL Prescription Yes AB
DURICEF CEFADROXIL/CEFADROXIL HEMIHYDRATEEQ 125MG BASE/5MLFOR SUSPENSION; ORAL Discontinued No None
DURICEF CEFADROXIL/CEFADROXIL HEMIHYDRATEEQ 250MG BASE/5MLFOR SUSPENSION; ORAL Prescription No AB


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