Visitor Monitoring Drug History: NEODECADRON
 
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: NEODECADRON
FDA Application No: (NDA) 050322
Active Ingredient(s): DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE
Company: MERCK
 
Label History
 
Labels are not available on this site for NEODECADRON, (NDA) 050322
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/29/1998 048Control Supplement  
8/31/1998 047Control Supplement  
2/24/1998 046Control Supplement  
12/23/1997 045Control Supplement  
4/16/1996 044Manufacturing Change or Addition  
4/25/1995 043Manufacturing Change or Addition  
5/5/1995 042Control Supplement  
1/13/1981 041Labeling Revision  
8/28/1980 040Labeling Revision  
8/6/1980 039Manufacturing Change or Addition  
3/27/1980 038Manufacturing Change or Addition  
2/27/1980 037Control Supplement  
3/28/1978 036Control Supplement  
1/24/1978 035Formulation Revision  
5/16/1977 034Labeling Revision  
4/18/1977 033Labeling Revision  
4/12/1977 032Labeling Revision  
3/15/1976 031Control Supplement  
1/9/1976 030Labeling Revision  
10/17/1975 029Control Supplement  
7/8/1975 028Formulation Revision  
12/17/1973 027Labeling Revision  
4/23/1973 026Control Supplement  
9/13/1972 025Labeling Revision  
7/18/1972 024Control Supplement  
4/27/1972 023Control Supplement  
6/18/1971 022Control Supplement  
4/21/1971 021Control Supplement  
4/30/1970 020Labeling Revision  
4/14/1970 019Package Change  
3/2/1970 018Control Supplement  
9/29/1995 017Labeling Revision  
9/29/1995 016Labeling Revision  
9/29/1995 015Labeling Revision  
9/29/1995 014Labeling Revision  
9/29/1995 013Labeling Revision  
12/15/1987 012Manufacturing Change or Addition  
4/3/1987 011Labeling Revision  
1/22/1986 010Control Supplement  
10/30/1985 009Manufacturing Change or Addition  
3/7/1985 008Labeling Revision  
6/27/1984 007Labeling Revision  
2/6/1970 006Control Supplement  
8/27/1984 005Control Supplement  
2/2/1984 004Manufacturing Change or Addition  
4/22/1983 003Control Supplement  
2/25/1983 002Control Supplement  
7/2/1969 000Approval  
 
There are no Therapeutic Equivalents
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