Visitor Monitoring Drug History: TIAZAC
 
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: TIAZAC
FDA Application No: (NDA) 020401
Active Ingredient(s): DILTIAZEM HYDROCHLORIDE
Company: BIOVAIL
 
Label History
 
Labels are not available on this site for TIAZAC, (NDA) 020401
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/21/2007 034Labeling Revision Letter 
10/3/2002 025Manufacturing Change or Addition  
11/26/2001 023Manufacturing Change or Addition  
9/24/2001 022Manufacturing Change or Addition  
11/29/2000 021Manufacturing Change or Addition  
7/3/2001 020Control Supplement  
3/24/2000 019Labeling Revision Review 
2/17/2000 018Manufacturing Change or Addition  
10/13/1999 016Control Supplement  
4/5/2000 015Labeling Revision  
2/17/1999 014Manufacturing Change or Addition  
10/16/1998 013Formulation Revision Review 
1/28/1999 012Control Supplement  
8/14/1997 011Manufacturing Change or Addition  
9/22/1997 010Manufacturing Change or Addition  
9/9/1997 009Package Change  
9/3/1997 008Manufacturing Change or Addition  
1/30/1998 007New or Modified Indication Review 
10/1/1997 006Labeling Revision  
6/26/1996 005Manufacturing Change or Addition  
3/14/1997 004Manufacturing Change or Addition  
5/16/1996 003Manufacturing Change or Addition  
5/29/1996 002Manufacturing Change or Addition  
7/23/1996 001Manufacturing Change or Addition  
9/11/1995 000Approval  
 
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