Visitor Monitoring Drug Details: DEMULEN 1/35-21
 
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Drug Details

Drug Name: DEMULEN 1/35-21
FDA Application No: (NDA) 018168
Active Ingredient(s): ETHINYL ESTRADIOL; ETHYNODIOL DIACETATE
Company: GD SEARLE LLC
Original Approval or Tentative Approval Date: December 30, 1981
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
 
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
DEMULEN 1/35-21 ETHINYL ESTRADIOL; ETHYNODIOL DIACETATE0.035MG; 1MGTABLET; ORAL-21 Prescription Yes AB


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