Visitor Monitoring Drug History: MUCOMYST
 
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: MUCOMYST
FDA Application No: (NDA) 013601
Active Ingredient(s): ACETYLCYSTEINE
Company: APOTHECON
 
Label History
 
Labels are not available on this site for MUCOMYST, (NDA) 013601
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/24/2001 053Manufacturing Change or Addition  
3/19/1997 052Labeling Revision  
4/21/1997 051Manufacturing Change or Addition  
4/5/1991 050Manufacturing Change or Addition  
7/13/1993 048Package Change  
1/16/1987 044Control Supplement  
6/18/1986 041Control Supplement  
3/2/1983 039Control Supplement  
11/20/1981 036Control Supplement  
1/31/1985 035General Efficacy (MarkIV)  
1/10/1980 034Control Supplement  
6/18/1979 033Control Supplement  
4/23/1979 032Control Supplement  
9/19/1978 031Control Supplement  
8/14/1978 030Control Supplement  
9/1/1978 029Labeling Revision  
2/8/1980 028Control Supplement  
12/8/1977 026Manufacturing Change or Addition  
10/6/1977 025Package Change  
9/15/1977 024Control Supplement  
9/2/1975 022Control Supplement  
4/18/1975 020Control Supplement  
4/10/1975 019Control Supplement  
8/19/1974 018Supplement  
9/14/1963 000Approval  
 
Therapeutic Equivalents
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