Visitor Monitoring Drug History: MYCIFRADIN
 
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: MYCIFRADIN
FDA Application No: (NDA) 050285
Active Ingredient(s): NEOMYCIN SULFATE
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for MYCIFRADIN, (NDA) 050285
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/28/1994 034Labeling Revision  
2/22/1994 032Control Supplement  
9/28/1992 031Labeling Revision  
8/23/1984 030Labeling Revision  
8/23/1984 029Labeling Revision  
2/5/1982 028Control Supplement  
4/1/1981 027Control Supplement  
4/18/1979 026Practioner Draft Labeling  
2/27/1979 025Control Supplement  
5/18/1978 024Formulation Revision  
1/26/1978 023Control Supplement  
5/10/1976 022Control Supplement  
12/8/1975 021Labeling Revision  
7/1/1975 020Control Supplement  
1/23/1975 019Package Change  
1/20/1975 018Labeling Revision  
11/11/1974 017Control Supplement  
5/28/1974 016Labeling Revision  
5/1/1974 015Control Supplement  
2/25/1974 014Package Change  
2/26/1973 013Control Supplement  
6/19/1972 012Labeling Revision  
4/26/1972 010Labeling Revision  
4/19/1972 009Control Supplement  
4/10/1972 008Package Change  
11/1/1971 007Labeling Revision  
4/26/1971 006Control Supplement  
3/18/1971 005Control Supplement  
2/25/1971 004Labeling Revision  
2/23/1971 003Labeling Revision  
7/11/1988 002Labeling Revision  
1/20/1983 001Control Supplement  
10/13/1970 000Approval  
 
Therapeutic Equivalents
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