Visitor Monitoring Drug History: NAPHCON FORTE
 
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Label and Approval History

Drug Name: NAPHCON FORTE
FDA Application No: (ANDA) 080229
Active Ingredient(s): NAPHAZOLINE HYDROCHLORIDE
Company: ALCON
 
Label History
 
Labels are not available on this site for NAPHCON FORTE, (ANDA) 080229
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/28/2000 025Microbiology  
3/23/1999 024Chemistry  
5/7/1999 023Chemistry  
3/4/1999 022Microbiology  
4/1/1996 021Chemistry  
1/25/1996 020Chemistry  
10/5/1995 019Microbiology  
8/4/1995 018Chemistry  
7/2/1996 017Labeling  
4/6/1993 016Labeling  
6/4/1993 015Chemistry  
6/4/1993 014Chemistry  
4/27/1989 013Chemistry  
8/6/1987 010Chemistry  
11/26/1982 009Chemistry  
11/26/1982 005Chemistry  
3/6/1974 000Approval  
 
Therapeutic Equivalents
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