Visitor Monitoring Drug History: OPTIMINE
 
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: OPTIMINE
FDA Application No: (NDA) 017601
Active Ingredient(s): AZATADINE MALEATE
Company: SCHERING
 
Label History
 
Labels are not available on this site for OPTIMINE, (NDA) 017601
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/4/2002 020Labeling Revision Letter 
3/22/2000 018Control Supplement  
7/1/1992 015Manufacturing Change or Addition  
4/20/1992 014Control Supplement  
1/24/1989 012Control Supplement  
4/6/1988 011Manufacturing Change or Addition  
5/1/1987 010Manufacturing Change or Addition  
3/6/1991 009Control Supplement  
7/8/1986 008Control Supplement  
2/6/1985 007Control Supplement  
8/25/1982 006Practioner Draft Labeling  
3/28/1980 005Expiration Date Change  
2/15/1980 004Package Change  
1/8/1980 003Labeling Revision  
7/12/1979 002Control Supplement  
5/22/1979 001Control Supplement  
3/29/1977 000Approval  
 
There are no Therapeutic Equivalents
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