Visitor Monitoring Drug History: PROCARDIA
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Label and Approval History

Drug Name: PROCARDIA
FDA Application No: (NDA) 018482
Active Ingredient(s): NIFEDIPINE
Company: PFIZER
 
Label History
 
Labels are not available on this site for PROCARDIA, (NDA) 018482
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/5/2000 044Package Change  
2/22/2002 043Labeling Revision Letter 
8/12/1997 042Labeling Revision  
4/21/1997 041Labeling Revision  
3/22/1996 040Labeling Revision  
3/29/1996 039Manufacturing Change or Addition  
9/28/1995 038Control Supplement  
5/30/1995 037Control Supplement  
11/30/1994 036Labeling Revision  
10/4/1995 035Labeling Revision  
4/4/1994 034Manufacturing Change or Addition  
7/9/1992 033Control Supplement  
5/18/1990 032Manufacturing Change or Addition  
2/9/1990 031Manufacturing Change or Addition  
10/5/1988 030Control Supplement  
6/6/1988 029Package Change  
1/13/1988 028Package Change  
6/12/1987 027Expiration Date Change  
6/3/1987 026Expiration Date Change  
10/4/1995 025Labeling Revision  
9/17/1986 024Manufacturing Change or Addition  
6/26/1986 022Manufacturing Change or Addition  
8/26/1985 021Labeling Revision  
8/26/1985 019Labeling Revision  
5/30/1985 018Control Supplement  
2/25/1985 017Labeling Revision  
11/20/1984 015General Efficacy (MarkIV)  
11/20/1984 013Package Change  
7/24/1986 012New Dosage Regimen  
3/22/1984 011Package Change  
7/24/1986 010Labeling Revision  
4/6/1984 009Expiration Date Change  
9/23/1983 007Control Supplement  
3/22/1983 006Labeling Revision  
3/10/1983 005Manufacturing Change or Addition  
3/10/1983 004Manufacturing Change or Addition  
1/7/1983 003Package Change  
6/17/1982 002Labeling Revision  
8/6/1982 001Package Change  
12/31/1981 000Approval  
 
©2019 Drugs That Causes a False Positive on a Drug Test