Visitor Monitoring Drug History: ACHROMYCIN V
 
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: ACHROMYCIN V
FDA Application No: (NDA) 050263
Active Ingredient(s): TETRACYCLINE HYDROCHLORIDE
Company: LEDERLE
 
Label History
 
Labels are not available on this site for ACHROMYCIN V, (NDA) 050263
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/22/1983 067Control Supplement  
9/30/1982 066Control Supplement  
5/21/1979 065Labeling Revision  
10/11/1978 064Control Supplement  
2/9/1976 063Formulation Revision  
6/19/1973 062Labeling Revision  
9/5/1972 061Labeling Revision  
9/29/1971 060Formulation Revision  
9/2/1971 059Formulation Revision  
7/26/1971 058Labeling Revision  
7/14/1971 057Labeling Revision  
10/26/1970 056Labeling Revision  
1/5/1970 055Formulation Revision  
7/23/1969 054Formulation Revision  
9/12/1968 053Formulation Revision  
5/24/1967 052Package Change  
2/17/1966 050Formulation Revision  
12/17/1966 049Formulation Revision  
11/29/1965 047Formulation Revision  
8/18/1964 046Labeling Revision  
8/10/1964 045Labeling Revision  
6/23/1964 044Labeling Revision  
6/19/1964 043Labeling Revision  
10/18/1963 040New or Modified Indication  
10/18/1963 039Labeling Revision  
6/18/1963 038Labeling Revision  
6/4/1963 037Labeling Revision  
5/27/1963 036Labeling Revision  
4/16/1962 034Formulation Revision  
2/13/1962 033Labeling Revision  
2/13/1962 032Labeling Revision  
10/30/1961 031Labeling Revision  
7/24/1961 030Labeling Revision  
5/31/1961 029Labeling Revision  
3/17/1961 028Labeling Revision  
3/15/1961 027Labeling Revision  
2/17/1961 026Formulation Revision  
1/31/1961 025Formulation Revision  
11/22/1960 024Formulation Revision  
10/1/1958 023Labeling Revision  
9/15/1958 022Labeling Revision  
6/13/1958 021Labeling Revision  
4/17/1958 020Formulation Revision  
4/18/1958 019Formulation Revision  
5/19/1959 018Expiration Date Change  
10/18/1957 017Labeling Revision  
10/18/1957 016Labeling Revision  
6/25/1957 014Formulation Revision  
6/25/1957 013Control Supplement  
5/15/1957 012Control Supplement  
5/15/1957 011Control Supplement  
1/25/1957 010Labeling Revision  
11/15/1991 007Labeling Revision  
11/15/1991 006Labeling Revision  
7/13/1955 004Control Supplement  
7/6/1955 003Control Supplement  
6/3/1955 001Control Supplement  
1/27/1955 000Approval  
 
Therapeutic Equivalents
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