Visitor Monitoring Drug Details: CEFUROXIME AND DEXTROSE IN DUPLEX CONTAINER
 
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Drug Details

Drug Name: CEFUROXIME AND DEXTROSE IN DUPLEX CONTAINER
FDA Application No: (NDA) 050780
Active Ingredient(s): CEFUROXIME SODIUM
Company: B BRAUN
Original Approval or Tentative Approval Date: February 21, 2001
Chemical Type: 5 New manufacturer
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
CEFUROXIME AND DEXTROSE IN DUPLEX CONTAINER CEFUROXIME SODIUMEQ 750MG BASE/VIALINJECTABLE; INJECTION Prescription Yes AP
CEFUROXIME AND DEXTROSE IN DUPLEX CONTAINER CEFUROXIME SODIUMEQ 1.5GM BASE/VIALINJECTABLE; INJECTION Prescription Yes AP


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