Visitor Monitoring Drug History: JUNEL FE 1/20
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: JUNEL FE 1/20
FDA Application No: (ANDA) 076081
Active Ingredient(s): ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
Company: BARR
 
Label History
 
Labels are not available on this site for JUNEL FE 120, (ANDA) 076081
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/18/2003 000Approval  
 
There are no Therapeutic Equivalents
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