Visitor Monitoring Drug History: LACRISERT
 
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: LACRISERT
FDA Application No: (NDA) 018771
Active Ingredient(s): HYDROXYPROPYL CELLULOSE
Company: ATON
 
Label History
 
View the label approved on March 20, 2002 for LACRISERT, (NDA) 018771


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
11/22/2002 013Control Supplement  
3/20/2002 012Labeling Revision Letter
Label 
6/2/1998 011Control Supplement  
10/9/1997 010Package Change  
6/15/1997 009Labeling Revision  
8/21/1995 008Control Supplement  
10/21/1994 007Control Supplement  
7/1/1988 006Manufacturing Change or Addition  
11/19/1987 005Manufacturing Change or Addition  
11/1/1988 004Labeling Revision  
11/1/1988 003Labeling Revision  
1/21/1983 002Expiration Date Change  
1/21/1983 001Control Supplement  
6/1/1981 000Approval  
 
There are no Therapeutic Equivalents
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