Visitor Monitoring Drug History: UNIPEN IN PLASTIC CONTAINER
 
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 IN PLASTIC CONTAINER
FDA Application No: (NDA) 050320
Active Ingredient(s): NAFCILLIN SODIUM
Company: WYETH AYERST
 
Label History
 
Labels are not available on this site for UNIPEN IN PLASTIC CONTAINER, (NDA) 050320
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/12/1982 070Labeling Revision  
5/12/1982 069Labeling Revision  
6/1/1981 068Labeling Revision  
6/1/1981 067Control Supplement  
4/8/1981 066Labeling Revision  
4/8/1981 065Control Supplement  
11/21/1980 064Labeling Revision  
8/20/1980 063Expiration Date Change  
7/30/1979 062Labeling Revision  
2/23/1979 061Labeling Revision  
2/23/1979 060Labeling Revision  
12/21/1978 059Labeling Revision  
12/21/1978 058Control Supplement  
4/28/1978 057Labeling Revision  
2/6/1978 056Labeling Revision  
12/22/1977 055Labeling Revision  
10/4/1977 054Labeling Revision  
1/19/1978 053Expiration Date Change  
1/19/1978 052Expiration Date Change  
8/10/1977 051Labeling Revision  
6/1/1977 050Control Supplement  
2/11/1977 049Labeling Revision  
6/20/1977 047Control Supplement  
1/11/1977 046Labeling Revision  
1/11/1977 045Labeling Revision  
9/23/1976 044Labeling Revision  
9/7/1976 043Labeling Revision  
9/7/1976 042Control Supplement  
3/23/1976 041Labeling Revision  
3/23/1976 040Labeling Revision  
3/23/1976 039Labeling Revision  
2/13/1976 038Labeling Revision  
5/22/1975 036Labeling Revision  
8/19/1975 035Labeling Revision  
1/23/1975 034Labeling Revision  
8/2/1974 031Labeling Revision  
3/12/1974 030Labeling Revision  
1/24/1974 029Labeling Revision  
11/23/1973 028Labeling Revision  
11/19/1973 027Labeling Revision  
1/11/1972 024Labeling Revision  
12/6/1971 023Labeling Revision  
10/22/1971 022Labeling Revision  
9/24/1971 021Control Supplement  
8/31/1972 020Labeling Revision  
5/19/1971 019Labeling Revision  
5/18/1971 018Labeling Revision  
4/2/1971 017Labeling Revision  
12/11/1970 016Labeling Revision  
8/10/1970 015Labeling Revision  
8/31/1988 012Control Supplement  
7/20/1988 011Labeling Revision  
12/19/1988 010Control Supplement  
2/22/1988 009Labeling Revision  
7/8/1987 008Labeling Revision  
4/14/1987 007Control Supplement  
8/27/1985 006Labeling Revision  
7/29/1987 005Control Supplement  
12/2/1986 004Manufacturing Change or Addition  
12/3/1985 003Control Supplement  
1/19/1983 002Control Supplement  
12/28/1982 001Labeling Revision  
6/23/1970 000Approval  
 
Therapeutic Equivalents
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