Visitor Monitoring Drug History: GRISACTIN
 
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: GRISACTIN
FDA Application No: (NDA) 050051
Active Ingredient(s): GRISEOFULVIN, MICROCRYSTALLINE
Company: WYETH AYERST
 
Label History
 
Labels are not available on this site for GRISACTIN, (NDA) 050051
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/9/1996 065Manufacturing Change or Addition  
5/26/1981 064Control Supplement  
5/20/1981 063Control Supplement  
2/19/1981 062Control Supplement  
12/31/1980 061Manufacturing Change or Addition  
8/27/1980 060Control Supplement  
6/24/1980 059Manufacturing Change or Addition  
1/21/1980 058Manufacturing Change or Addition  
11/8/1979 057Control Supplement  
11/8/1979 056Control Supplement  
10/18/1978 055Manufacturing Change or Addition  
6/21/1977 054Manufacturing Change or Addition  
6/10/1977 053Package Change  
10/29/1976 052Manufacturing Change or Addition  
10/16/1974 051Manufacturing Change or Addition  
5/13/1976 050Control Supplement  
4/1/1976 049Control Supplement  
11/11/1975 048Control Supplement  
9/30/1975 047Control Supplement  
6/5/1974 046Control Supplement  
5/22/1974 045Package Change  
2/22/1974 044Package Change  
2/12/1973 043Manufacturing Change or Addition  
2/2/1973 042Manufacturing Change or Addition  
6/16/1972 041Labeling Revision  
5/3/1972 040Labeling Revision  
3/27/1972 039Control Supplement  
2/3/1972 038Package Change  
6/20/1972 037Control Supplement  
11/12/1971 035Labeling Revision  
9/13/1971 034Labeling Revision  
6/28/1971 033Labeling Revision  
6/3/1971 032Package Change  
7/29/1969 031Manufacturing Change or Addition  
7/15/1969 030Expiration Date Change  
7/15/1969 029Expiration Date Change  
4/24/1969 028Manufacturing Change or Addition  
7/27/1967 027Labeling Revision  
10/28/1966 025Control Supplement  
9/27/1966 024Expiration Date Change  
5/16/1966 023Control Supplement  
4/29/1966 022Labeling Revision  
5/2/1966 021Labeling Revision  
5/2/1966 020Labeling Revision  
3/18/1966 019Labeling Revision  
3/15/1966 018Expiration Date Change  
3/14/1966 017Expiration Date Change  
2/7/1966 016Labeling Revision  
11/2/1965 015Labeling Revision  
4/26/1965 014Expiration Date Change  
11/24/1964 013Expiration Date Change  
9/21/1964 011Labeling Revision  
6/24/1964 010Manufacturing Change or Addition  
3/16/1965 009Labeling Revision  
8/4/1964 007Labeling Revision  
1/28/1993 005Manufacturing Change or Addition  
7/29/1987 004Package Change  
1/12/1984 002Control Supplement  
6/29/1983 001Control Supplement  
8/22/1962 000Approval  
 
There are no Therapeutic Equivalents
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