Visitor Monitoring Drug History: ZOVIA 1/50E-21
 
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Label and Approval History

Drug Name: ZOVIA 1/50E-21
FDA Application No: (ANDA) 072722
Active Ingredient(s): ETHINYL ESTRADIOL; ETHYNODIOL DIACETATE
Company: WATSON LABS
 
Label History
 
Labels are not available on this site for ZOVIA 150E21, (ANDA) 072722
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/30/2002 011Control Supplement  
10/18/2002 010Control Supplement  
10/9/2001 009Facility Addition  
1/29/2001 007Control Supplement  
9/11/2002 006Labeling  
4/30/1997 005Labeling  
4/10/1996 004Labeling  
9/27/1994 003Labeling  
8/12/1993 002Labeling  
5/17/1993 001Labeling  
12/30/1991 000Approval  
 
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