Visitor Monitoring Drug Details: CEFADROXIL
 
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Drug Details

Drug Name: CEFADROXIL
FDA Application No: (ANDA) 065115
Active Ingredient(s): CEFADROXIL/CEFADROXIL HEMIHYDRATE
Company: RANBAXY
Original Approval or Tentative Approval Date: March 26, 2003
 
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
CEFADROXIL CEFADROXIL/CEFADROXIL HEMIHYDRATEEQ 125MG BASE/5MLFOR SUSPENSION; ORAL Prescription Yes None
CEFADROXIL CEFADROXIL/CEFADROXIL HEMIHYDRATEEQ 250MG BASE/5MLFOR SUSPENSION; ORAL Prescription No AB
CEFADROXIL CEFADROXIL/CEFADROXIL HEMIHYDRATEEQ 500MG BASE/5MLFOR SUSPENSION; ORAL Prescription No AB


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