Visitor Monitoring Drug Details: VANCOLED
 
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Drug Details

Drug Name: VANCOLED
FDA Application No: (ANDA) 063321
Active Ingredient(s): VANCOMYCIN HYDROCHLORIDE
Company: LEDERLE
Original Approval or Tentative Approval Date: October 15, 1993
 
Therapeutic Equivalents Labels are not available
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
VANCOLED VANCOMYCIN HYDROCHLORIDEEQ 250MG BASE/5MLFOR SOLUTION; ORAL Discontinued No None
VANCOLED VANCOMYCIN HYDROCHLORIDEEQ 500MG BASE/6MLFOR SOLUTION; ORAL Discontinued No None


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