Visitor Monitoring Drug History: OPHTHETIC
 
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: OPHTHETIC
FDA Application No: (NDA) 012583
Active Ingredient(s): PROPARACAINE HYDROCHLORIDE
Company: ALLERGAN
 
Label History
 
View the label approved on June 20, 2002 for OPHTHETIC, (NDA) 012583


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
4/12/2002 038Control Supplement  
6/20/2002 037Manufacturing Change or Addition Letter
Label 
4/12/2001 035Manufacturing Change or Addition  
3/12/2001 034Control Supplement  
10/2/2000 033Manufacturing Change or Addition  
10/17/1997 032Control Supplement  
9/18/1997 031Control Supplement  
3/17/1997 030Control Supplement  
5/5/1995 029Control Supplement  
6/20/2002 028Labeling Revision Letter
Label 
8/3/1995 027Control Supplement  
3/4/1993 026Formulation Revision  
2/5/1990 025Manufacturing Change or Addition  
2/5/1990 024Control Supplement  
3/20/1989 023Control Supplement  
10/13/1989 022Manufacturing Change or Addition  
4/21/1987 019Practioner Draft Labeling  
5/21/1982 018Manufacturing Change or Addition  
5/21/1982 017Manufacturing Change or Addition  
5/22/1980 016Manufacturing Change or Addition  
10/4/1979 015Control Supplement  
7/14/1977 011Control Supplement  
9/23/1976 010Labeling Revision  
9/10/1976 009Control Supplement  
9/23/1976 008Labeling Revision  
9/10/1976 007Control Supplement  
9/17/1975 006Labeling Revision  
7/1/1975 005Control Supplement  
1/23/1961 000Approval  
 
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