Visitor Monitoring Drug History: CAVERJECT
 
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: CAVERJECT
FDA Application No: (NDA) 020379
Active Ingredient(s): ALPROSTADIL
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for CAVERJECT, (NDA) 020379
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/2/2003 017Labeling Revision Letter 
10/15/2002 016Control Supplement  
3/29/2001 015Manufacturing Change or Addition  
4/3/2000 014Manufacturing Change or Addition  
11/29/2000 013Control Supplement  
7/2/1999 012Labeling Revision  
1/15/2002 011Labeling Revision Letter 
1/20/1999 010Labeling Revision  
3/26/1998 009Labeling Revision Review 
5/20/1998 008Control Supplement  
5/19/1997 007Control Supplement  
10/8/1997 006Labeling Revision  
10/21/1996 005Labeling Revision  
6/28/1996 004Labeling Revision  
6/27/1996 003Formulation Revision  
5/13/1996 002Control Supplement  
3/19/1996 001Control Supplement  
7/6/1995 000Approval  
 
Therapeutic Equivalents
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