Visitor Monitoring Drug History: DILACOR XR
 
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: DILACOR XR
FDA Application No: (NDA) 020092
Active Ingredient(s): DILTIAZEM HYDROCHLORIDE
Company: WATSON LABS
 
Label History
 
Labels are not available on this site for DILACOR XR, (NDA) 020092
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/12/2003 015Labeling Revision Letter 
8/7/2001 014Manufacturing Change or Addition  
10/28/1998 011Manufacturing Change or Addition  
3/20/1996 010Control Supplement  
10/31/1995 009Manufacturing Change or Addition  
2/2/1995 008Manufacturing Change or Addition  
2/9/1995 007Package Change  
2/9/1995 006Manufacturing Change or Addition  
3/2/1995 005New or Modified Indication  
12/6/1993 004Labeling Revision  
6/19/1997 003Labeling Revision  
10/15/1992 002Labeling Revision  
10/2/1992 001Labeling Revision  
5/29/1992 000Approval  
 
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