Visitor Monitoring Drug History: DECLOMYCIN
 
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Label and Approval History

Drug Name: DECLOMYCIN
FDA Application No: (NDA) 050262
Active Ingredient(s): DEMECLOCYCLINE HYDROCHLORIDE
Company: LEDERLE
 
Label History
 
Labels are not available on this site for DECLOMYCIN, (NDA) 050262
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/28/1974 061Control Supplement  
10/1/1973 060Labeling Revision  
3/26/1982 059Control Supplement  
10/18/1979 058Formulation Revision  
5/26/1976 057Control Supplement  
2/9/1976 056Control Supplement  
3/10/1975 055Control Supplement  
9/5/1972 054Labeling Revision  
2/10/1972 053Package Change  
1/3/1969 051Control Supplement  
10/12/1967 050Labeling Revision  
7/13/1967 049Labeling Revision  
7/13/1967 048Labeling Revision  
1/5/1966 047Labeling Revision  
9/28/1966 046Labeling Revision  
10/19/1965 045Control Supplement  
9/3/1965 044Control Supplement  
9/3/1965 043Control Supplement  
8/21/1965 042Control Supplement  
3/16/1965 041Control Supplement  
2/25/1965 040Control Supplement  
2/9/1965 039Expiration Date Change  
1/20/1972 038Labeling Revision  
7/13/1971 037Labeling Revision  
9/14/1967 036Labeling Revision  
6/16/1967 035Labeling Revision  
12/28/1965 034Labeling Revision  
9/3/1965 033Labeling Revision  
3/16/1965 032Labeling Revision  
8/13/1964 031Labeling Revision  
6/9/1964 030Labeling Revision  
1/15/1964 029Labeling Revision  
1/14/1964 028Labeling Revision  
11/12/1963 027Labeling Revision  
7/10/1963 026Labeling Revision  
5/24/1963 025Labeling Revision  
1/11/1962 024Labeling Revision  
10/30/1961 023Labeling Revision  
2/15/1960 021Labeling Revision  
8/2/1965 020Labeling Revision  
11/21/1963 019Control Supplement  
8/21/1961 018Control Supplement  
8/21/1961 017New or Modified Indication  
8/21/1961 016New or Modified Indication  
6/23/1961 015Formulation Revision  
12/19/1960 014Formulation Revision  
11/29/1960 013Formulation Revision  
4/12/1960 012New Dosage Regimen  
3/4/1960 011New Dosage Regimen  
11/20/1991 008Labeling Revision  
11/20/1991 006Labeling Revision  
10/9/1986 005Labeling Revision  
6/21/1983 002Control Supplement  
1/14/1960 000Approval  
 
There are no Therapeutic Equivalents
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