Visitor Monitoring Drug History: DECLOMYCIN
 
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: DECLOMYCIN
FDA Application No: (NDA) 050261
Active Ingredient(s): DEMECLOCYCLINE HYDROCHLORIDE
Company: STIEFEL
 
Label History
 
Labels are not available on this site for DECLOMYCIN, (NDA) 050261
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/18/2003 097Labeling Revision Letter 
5/1/2003 095Labeling Revision Letter 
12/18/2003 094Labeling Revision Letter 
12/7/2000 093Control Supplement  
10/20/1999 092Control Supplement  
6/25/1997 091Manufacturing Change or Addition  
6/25/1997 090Package Change  
3/26/1982 089Package Change  
4/8/1980 088Control Supplement  
5/16/1979 087Control Supplement  
9/20/1978 086Formulation Revision  
9/14/1978 085Expiration Date Change  
6/7/1978 084Labeling Revision  
8/25/1976 083Control Supplement  
6/25/1976 082Expiration Date Change  
3/22/1976 081Control Supplement  
12/29/1975 080Control Supplement  
7/8/1975 079Control Supplement  
4/25/1974 078Expiration Date Change  
2/28/1974 077Labeling Revision  
1/10/1974 076Formulation Revision  
10/1/1973 075Labeling Revision  
10/1/1973 074Labeling Revision  
10/1/1973 073Labeling Revision  
2/16/1972 072Package Change  
2/16/1972 071Package Change  
2/16/1972 070Labeling Revision  
1/10/1972 069Labeling Revision  
1/10/1972 068Labeling Revision  
1/10/1972 067Labeling Revision  
7/14/1971 066Labeling Revision  
6/14/1971 065Formulation Revision  
12/1/1970 064Formulation Revision  
10/23/1970 063Expiration Date Change  
10/23/1970 062Expiration Date Change  
4/14/1970 061Formulation Revision  
1/3/1969 060Package Change  
12/7/1967 059Labeling Revision  
11/17/1967 058Labeling Revision  
4/25/1967 057Labeling Revision  
4/25/1967 056Labeling Revision  
4/25/1967 055Labeling Revision  
2/15/1967 054Labeling Revision  
2/20/1967 053Labeling Revision  
12/29/1966 052Package Change  
12/29/1966 051Package Change  
11/29/1966 050Labeling Revision  
9/28/1966 046Labeling Revision  
9/28/1966 045Labeling Revision  
12/5/1966 044Labeling Revision  
9/15/1966 043Formulation Revision  
7/6/1966 042Labeling Revision  
6/3/1966 041Labeling Revision  
5/4/1966 040Labeling Revision  
5/4/1966 039Labeling Revision  
5/4/1966 038Labeling Revision  
5/4/1966 037Labeling Revision  
5/4/1966 036Labeling Revision  
5/4/1966 035Labeling Revision  
5/4/1966 034Labeling Revision  
5/4/1966 033Labeling Revision  
5/4/1966 032Labeling Revision  
5/4/1966 031Labeling Revision  
3/25/1966 030Labeling Revision  
3/11/1966 029Labeling Revision  
2/18/1966 028Labeling Revision  
3/14/1966 027Labeling Revision  
1/5/1966 026Labeling Revision  
1/5/1966 025Labeling Revision  
12/22/1965 024Labeling Revision  
1/13/1966 023Labeling Revision  
1/13/1966 022Labeling Revision  
12/7/1965 021Labeling Revision  
12/13/1965 020Labeling Revision  
12/23/1965 019New Dosage Regimen  
8/19/1965 018Labeling Revision  
9/24/1965 017Package Change  
5/14/1965 016Manufacturing Change or Addition  
5/14/1965 015Manufacturing Change or Addition  
3/11/1965 014Labeling Revision  
11/20/1991 011Labeling Revision  
12/17/1987 006Formulation Revision  
10/9/1986 005Labeling Revision  
2/10/1965 003Labeling Revision  
6/21/1983 002Control Supplement  
9/22/1964 000Approval  
 
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