Visitor Monitoring Drug History: MAXITROL
 
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: MAXITROL
FDA Application No: (NDA) 050023
Active Ingredient(s): DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Company: FALCON PHARMS
 
Label History
 
Labels are not available on this site for MAXITROL, (NDA) 050023
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/11/2002 023Control Supplement  
12/4/2002 022Control Supplement  
10/10/2000 021Manufacturing Change or Addition  
2/25/2000 020Manufacturing Change or Addition  
8/17/1999 019Control Supplement  
2/5/1999 018Manufacturing Change or Addition  
3/11/1999 017Control Supplement  
8/4/1998 016Control Supplement  
3/18/1996 014Control Supplement  
11/1/1995 013Control Supplement  
11/1/1995 012Control Supplement  
8/30/1995 011Labeling Revision  
7/27/1994 010Control Supplement  
1/22/1993 009Manufacturing Change or Addition  
6/13/1995 008Package Change  
3/3/1989 006Control Supplement  
3/25/1977 005Control Supplement  
3/1/1976 004Control Supplement  
2/20/1973 003Control Supplement  
10/14/1971 002Control Supplement  
12/14/1966 001Expiration Date Change  
6/6/1963 000Approval  
 
There are no Therapeutic Equivalents
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