Visitor Monitoring Drug History: DEPO-PROVERA
 
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: DEPO-PROVERA
FDA Application No: (NDA) 012541
Active Ingredient(s): MEDROXYPROGESTERONE ACETATE
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for DEPOPROVERA, (NDA) 012541
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/3/2000 069Manufacturing Change or Addition  
11/28/1997 067Labeling Revision  
11/28/1995 066Control Supplement  
4/18/1995 065Control Supplement  
4/12/1995 064Package Change  
7/27/1994 063Control Supplement  
6/16/1994 062Control Supplement  
2/17/1994 061Control Supplement  
2/18/1994 060Labeling Revision  
6/23/1993 058Control Supplement  
9/7/1995 057Labeling Revision  
2/20/1990 056Labeling Revision  
5/20/1980 049Manufacturing Change or Addition  
12/4/1978 042Labeling Revision  
11/1/1976 041Expiration Date Change  
11/1/1976 039Control Supplement  
11/1/1976 038Labeling Revision  
1/19/1979 037Control Supplement  
9/23/1960 000Approval  
 
There are no Therapeutic Equivalents
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