Visitor Monitoring Drug Details: GENCEPT 10/11-21
 
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Drug Details

Drug Name: GENCEPT 10/11-21
FDA Application No: (ANDA) 072694
Active Ingredient(s): ETHINYL ESTRADIOL; NORETHINDRONE
Company: BARR
Original Approval or Tentative Approval Date: February 28, 1992
 
 
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
GENCEPT 10/11-21 ETHINYL ESTRADIOL; NORETHINDRONE0.035MG,0.035MG; 0.5MG,1MGTABLET; ORAL-21 Prescription No AB


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