Visitor Monitoring Drug Details: KEFLET
 
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Drug Details

Drug Name: KEFLET
FDA Application No: (NDA) 050440
Active Ingredient(s): CEPHALEXIN
Company: LILLY
Original Approval or Tentative Approval Date: October 12, 1972
 
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
KEFLET CEPHALEXINEQ 500MG BASETABLET; ORAL Discontinued No None
KEFLET CEPHALEXINEQ 1GM BASETABLET; ORAL Discontinued No None
KEFLET CEPHALEXINEQ 250MG BASETABLET; ORAL Discontinued No None


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