Visitor Monitoring Drug History: ISOPTIN SR
 
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: ISOPTIN SR
FDA Application No: (NDA) 019152
Active Ingredient(s): VERAPAMIL HYDROCHLORIDE
Company: RANBAXY
 
Label History
 
Labels are not available on this site for ISOPTIN SR, (NDA) 019152
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/26/2002 030Control Supplement Letter 
2/14/2001 029Control Supplement  
2/12/2001 028Expiration Date Change  
7/14/2000 027Manufacturing Change or Addition  
9/28/2001 026Labeling Revision  
12/11/1998 025Manufacturing Change or Addition  
5/16/1997 024Manufacturing Change or Addition  
1/13/1998 023Labeling Revision  
11/5/1993 022Package Change  
3/17/1995 020Manufacturing Change or Addition  
9/23/1992 019Expiration Date Change  
9/3/1992 017Labeling Revision  
5/4/1992 016Expiration Date Change  
7/28/1994 015Manufacturing Change or Addition  
3/6/1991 014Formulation Revision  
1/19/1990 013Manufacturing Change or Addition  
5/17/1989 012Package Change  
3/30/1989 011Manufacturing Change or Addition  
6/14/1989 010Package Change  
12/15/1989 009New Dosage Regimen  
9/22/1988 008Labeling Revision  
8/8/1989 007Package Change  
3/6/1991 006Manufacturing Change or Addition  
7/20/1988 005Labeling Revision  
11/30/1988 004Manufacturing Change or Addition  
11/30/1988 003Manufacturing Change or Addition  
11/30/1988 002Manufacturing Change or Addition  
9/24/1987 001Package Change  
12/16/1986 000Approval  
 
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