Visitor Monitoring Drug History: CARTIA XT
 
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: CARTIA XT
FDA Application No: (ANDA) 074752
Active Ingredient(s): DILTIAZEM HYDROCHLORIDE
Company: ANDRX PHARMS
 
Label History
 
View the label approved on July 9, 1998 for CARTIA XT, (ANDA) 074752


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/18/2003 018Supplement Review 
12/24/2002 017Packager Addition Review 
10/11/2002 016Packager Addition Review 
2/27/2002 015Control Supplement Review 
1/8/2001 013Manufacturing Revision Review 
1/8/2001 012Control Supplement Review 
8/16/2000 011Control Supplement Review 
5/12/2000 009Supplier Addition Review 
7/18/2000 008Supplier Addition Review 
6/8/1999 007Labeling Review 
6/8/1999 006Labeling Review 
4/2/1999 005Labeling Review 
6/8/1999 004Chemistry Review 
6/8/1999 003Chemistry Review 
6/8/1999 002Chemistry Review 
6/8/1999 001Chemistry Review 
7/9/1998 000Approval Letter
Label
Review 
9/15/1997 000Tentative Approval Letter
Label
Review 
 
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