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) 050324
Active Ingredient(s): DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE
Company: MERCK
 
Label History
 
Labels are not available on this site for NEODECADRON, (NDA) 050324
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/16/1996 032Manufacturing Change or Addition  
6/12/1995 031Control Supplement  
9/6/1984 030Manufacturing Change or Addition  
7/20/1982 029Labeling Revision  
10/13/1981 028Labeling Revision  
9/29/1981 027Control Supplement  
9/29/1981 025Manufacturing Change or Addition  
1/13/1981 024Labeling Revision  
8/28/1980 023Labeling Revision  
4/1/1980 022Control Supplement  
2/17/1978 021Control Supplement  
1/27/1978 020New or Modified Indication  
3/23/1977 019Labeling Revision  
2/23/1976 018Control Supplement  
1/9/1976 017New or Modified Indication  
3/7/1975 016Formulation Revision  
12/18/1973 015Labeling Revision  
9/7/1972 014Labeling Revision  
8/31/1972 013Package Change  
11/20/1995 012Labeling Revision  
11/20/1995 011Labeling Revision  
3/11/1992 010Manufacturing Change or Addition  
11/20/1995 009Labeling Revision  
11/20/1995 008Labeling Revision  
12/15/1987 007Manufacturing Change or Addition  
4/30/1970 006Labeling Revision  
12/24/1969 005Control Supplement  
9/6/1984 004Control Supplement  
7/10/1984 003Labeling Revision  
11/3/1969 002Labeling Revision  
2/28/1984 001Manufacturing Change or Addition  
9/15/1969 000Approval  
 
There are no Therapeutic Equivalents
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