Visitor Monitoring Drug Details: CEPHRADINE
 
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Drug Details

Drug Name: CEPHRADINE
FDA Application No: (ANDA) 062683
Active Ingredient(s): CEPHRADINE
Company: TEVA
Original Approval or Tentative Approval Date: January 9, 1987
 
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
CEPHRADINE CEPHRADINE250MGCAPSULE; ORAL Discontinued No None
CEPHRADINE CEPHRADINE500MGCAPSULE; ORAL Discontinued No None


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