Visitor Monitoring Drug Details: ANSPOR
 
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Drug Details

Drug Name: ANSPOR
FDA Application No: (ANDA) 061859
Active Ingredient(s): CEPHRADINE
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: October 1, 1974
 
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
ANSPOR CEPHRADINE250MGCAPSULE; ORAL Discontinued No None
ANSPOR CEPHRADINE500MGCAPSULE; ORAL Discontinued No None


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