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

Drug Name: NAPHCON-A
FDA Application No: (NDA) 020226
Active Ingredient(s): NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE
Company: ALCON
 
Label History
 
Labels are not available on this site for NAPHCONA, (NDA) 020226
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/4/2002 018Control Supplement  
3/16/2001 017Control Supplement  
9/22/2000 016Manufacturing Change or Addition  
3/17/2000 015Package Change  
1/21/2000 014Manufacturing Change or Addition  
11/19/1999 013Manufacturing Change or Addition  
10/4/1999 012Control Supplement  
6/14/1999 011Manufacturing Change or Addition  
12/16/1999 010Control Supplement  
8/20/1998 009Control Supplement  
12/23/1997 008Manufacturing Change or Addition  
9/26/1996 007Labeling Revision  
4/16/1996 006Control Supplement  
7/30/1996 005Labeling Revision  
11/1/1995 004Control Supplement  
11/1/1995 003Control Supplement  
2/23/1995 002Labeling Revision  
10/4/1994 001Labeling Revision  
6/8/1994 000Approval  
 
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