Visitor Monitoring Drug History: UNIPEN
 
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: UNIPEN
FDA Application No: (NDA) 050111
Active Ingredient(s): NAFCILLIN SODIUM
Company: WYETH AYERST
 
Label History
 
Labels are not available on this site for UNIPEN, (NDA) 050111
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/30/1996 028Manufacturing Change or Addition  
9/28/1987 026Labeling Revision  
1/20/1987 025Package Change  
12/5/1986 024Control Supplement  
9/5/1985 023New or Modified Indication  
12/28/1982 022Labeling Revision  
10/2/1980 021Package Change  
4/24/1978 020Control Supplement  
12/22/1977 019Labeling Revision  
2/11/1977 018Labeling Revision  
1/27/1976 017Labeling Revision  
10/3/1975 016Package Change  
8/19/1975 015Labeling Revision  
6/24/1974 014Labeling Revision  
5/13/1974 013Labeling Revision  
3/27/1974 012Control Supplement  
3/12/1974 011Labeling Revision  
3/8/1974 010Package Change  
2/22/1974 009Control Supplement  
1/23/1974 008Labeling Revision  
8/14/1973 007Labeling Revision  
4/10/1991 006Labeling Revision  
7/24/1973 005Labeling Revision  
8/1/1972 004Control Supplement  
10/28/1971 003Labeling Revision  
10/22/1971 002Labeling Revision  
4/22/1971 001Labeling Revision  
4/7/1970 000Approval  
 
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