Visitor Monitoring Drug History: PROCARDIA XL
 
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Label and Approval History

Drug Name: PROCARDIA XL
FDA Application No: (NDA) 019684
Active Ingredient(s): NIFEDIPINE
Company: PFIZER
 
Label History
 
Labels are not available on this site for PROCARDIA XL, (NDA) 019684
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/5/2000 017Package Change  
8/18/1998 015Package Change  
8/12/1997 014Labeling Revision  
4/21/1997 013Labeling Revision  
1/8/1997 012Labeling Revision Review 
3/29/1996 011Manufacturing Change or Addition  
11/30/1994 010Labeling Revision  
12/26/1995 009Labeling Revision  
4/4/1994 008Manufacturing Change or Addition  
3/18/1991 006Formulation Revision  
9/14/1990 005Labeling Revision  
5/18/1990 004Manufacturing Change or Addition  
2/9/1990 003Manufacturing Change or Addition  
3/8/1990 002Package Change  
11/13/1989 001Manufacturing Change or Addition  
9/6/1989 000Approval  
 
Therapeutic Equivalents
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