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) 050199
Active Ingredient(s): NAFCILLIN SODIUM
Company: WYETH AYERST
 
Label History
 
Labels are not available on this site for UNIPEN, (NDA) 050199
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/28/1982 026Control Supplement  
10/22/1980 025Package Change  
10/3/1980 024Labeling Revision  
10/2/1980 023Labeling Revision  
5/15/1980 022Control Supplement  
4/24/1978 021Control Supplement  
4/18/1978 020Control Supplement  
12/22/1977 019Labeling Revision  
10/15/1976 018Manufacturing Change or Addition  
9/7/1976 017Labeling Revision  
5/4/1976 016Control Supplement  
7/26/1976 015Formulation Revision  
7/26/1976 014Formulation Revision  
4/11/1974 013Package Change  
1/24/1973 012Control Supplement  
5/6/1970 011Control Supplement  
5/6/1970 010Expiration Date Change  
10/16/1967 009Expiration Date Change  
8/5/1966 008Control Supplement  
3/10/1966 007Control Supplement  
5/14/1991 006Package Change  
4/10/1991 005Labeling Revision  
9/15/1987 004Labeling Revision  
12/5/1986 003Labeling Revision  
8/27/1985 002Labeling Revision  
12/28/1982 001Labeling Revision  
10/11/1965 000Approval  
 
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