Visitor Monitoring Drug History: OCUPRESS
 
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: OCUPRESS
FDA Application No: (NDA) 019972
Active Ingredient(s): CARTEOLOL HYDROCHLORIDE
Company: NOVARTIS
 
Label History
 
Labels are not available on this site for OCUPRESS, (NDA) 019972
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/22/2001 018Control Supplement  
3/29/2001 017Control Supplement  
12/26/2000 016Manufacturing Change or Addition  
12/18/1998 015Manufacturing Change or Addition  
11/24/1997 014Manufacturing Change or Addition  
10/22/1996 013Control Supplement  
2/20/1997 012Expiration Date Change  
8/6/1996 011Manufacturing Change or Addition  
8/6/1996 010Manufacturing Change or Addition  
4/1/1996 009Control Supplement  
7/31/1996 008Package Change  
5/20/1996 007Control Supplement  
5/20/1996 006Package Change  
5/20/1996 005Package Change  
3/18/1996 004Control Supplement  
3/18/1996 003Control Supplement  
4/16/1996 002Control Supplement  
5/23/1990 000Approval  
 
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