Visitor Monitoring Drug Details: ERYTHROMYCIN
 
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Drug Details

Drug Name: ERYTHROMYCIN
FDA Application No: (ANDA) 061621
Active Ingredient(s): ERYTHROMYCIN
Company: ABBOTT
Original Approval or Tentative Approval Date: July 11, 1972
 
There are no 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
ERYTHROMYCIN ERYTHROMYCIN250MGTABLET; ORAL Prescription No None
ERYTHROMYCIN ERYTHROMYCIN500MGTABLET; ORAL Prescription Yes None


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