Visitor Monitoring Drug History: CARDIZEM CD
 
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: CARDIZEM CD
FDA Application No: (NDA) 020062
Active Ingredient(s): DILTIAZEM HYDROCHLORIDE
Company: BIOVAIL
 
Label History
 
Labels are not available on this site for CARDIZEM CD, (NDA) 020062
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/4/2001 033Control Supplement  
1/21/2000 032Control Supplement  
12/3/1999 031Manufacturing Change or Addition  
10/19/1999 030Control Supplement  
11/18/1999 029Manufacturing Change or Addition  
4/29/1999 028Control Supplement  
8/24/1999 027Formulation Revision Review 
4/15/1999 026Control Supplement  
3/21/2003 025Labeling Revision  
4/7/1998 024Control Supplement  
11/21/1997 023Manufacturing Change or Addition  
8/6/1997 022Control Supplement  
4/2/1996 021Labeling Revision  
4/2/1996 019Labeling Revision  
10/31/1995 018Control Supplement  
5/11/1995 017Control Supplement  
11/22/1994 016Control Supplement  
5/4/1995 015Control Supplement  
10/24/1994 014Control Supplement  
9/25/1995 013Package Change  
9/28/1994 012Package Change  
9/14/1994 011Manufacturing Change or Addition  
4/3/1995 010Package Change  
5/5/1994 009Control Supplement  
11/1/1993 008Control Supplement  
10/6/1993 007Labeling Revision  
6/29/1993 006Control Supplement  
4/28/1993 005Labeling Revision  
9/18/1992 004Manufacturing Change or Addition  
8/10/1992 003New Dosage Regimen  
8/4/1992 002Manufacturing Change or Addition  
10/15/1992 001New or Modified Indication  
12/27/1991 000Approval  
 
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