Visitor Monitoring Drug History: SPECTAZOLE
 
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: SPECTAZOLE
FDA Application No: (NDA) 018751
Active Ingredient(s): ECONAZOLE NITRATE
Company: JOHNSON AND JOHNSON
 
Label History
 
Labels are not available on this site for SPECTAZOLE, (NDA) 018751
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/11/2001 019Control Supplement  
4/4/2001 018Control Supplement  
3/20/2001 017Package Change  
7/23/1998 016Manufacturing Change or Addition  
11/17/1995 012Manufacturing Change or Addition  
2/24/1995 011Labeling Revision  
9/10/1992 009Control Supplement  
3/9/1990 008Control Supplement  
4/25/1990 006Labeling Revision  
12/18/1986 005Manufacturing Change or Addition  
6/28/1985 004Package Change  
1/8/1985 002Control Supplement  
5/22/1985 001Labeling Revision  
12/23/1982 000Approval  
 
Therapeutic Equivalents
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