Visitor Monitoring Drug History: ENLON-PLUS
 
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: ENLON-PLUS
FDA Application No: (NDA) 019677
Active Ingredient(s): ATROPINE SULFATE; EDROPHONIUM CHLORIDE
Company: BAXTER HLTHCARE CORP
 
Label History
 
View the label approved on December 15, 2005 for ENLONPLUS, (NDA) 019677


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
12/6/2005 005Labeling Revision Letter
Label 
4/18/2002 004Control Supplement  
12/26/2000 003Manufacturing Change or Addition  
3/11/1994 002Control Supplement  
3/20/1992 001Manufacturing Change or Addition  
11/6/1991 000Approval  
 
There are no Therapeutic Equivalents
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