Visitor Monitoring Drug History: VASOCON-A
 
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Label and Approval History

Drug Name: VASOCON-A
FDA Application No: (NDA) 018746
Active Ingredient(s): ANTAZOLINE PHOSPHATE; NAPHAZOLINE HYDROCHLORIDE
Company: NOVARTIS
 
Label History
 
Labels are not available on this site for VASOCONA, (NDA) 018746
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/2/2001 011Manufacturing Change or Addition  
3/6/1997 009Labeling Revision  
3/13/1995 008Labeling Revision  
8/3/1995 007Manufacturing Change or Addition  
7/11/1994 006OTC Labeling  
8/22/1995 004Control Supplement  
9/21/1990 001Manufacturing Change or Addition  
4/30/1990 000Approval  
 
There are no Therapeutic Equivalents
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