Visitor Monitoring Drug History: ACHROMYCIN
 
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
FDA Application No: (NDA) 050276
Active Ingredient(s): PROCAINE HYDROCHLORIDE; TETRACYCLINE HYDROCHLORIDE
Company: LEDERLE
 
Label History
 
Labels are not available on this site for ACHROMYCIN, (NDA) 050276
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/9/1986 045Labeling Revision  
9/30/1985 044Control Supplement  
8/28/1984 043Manufacturing Change or Addition  
7/24/1984 042Control Supplement  
3/22/1982 040Labeling Revision  
5/12/1981 039Control Supplement  
3/20/1981 038Control Supplement  
9/18/1979 037Control Supplement  
6/7/1978 036Labeling Revision  
1/13/1975 035Control Supplement  
4/26/1974 034Control Supplement  
6/21/1973 033Labeling Revision  
10/21/1973 032Formulation Revision  
1/5/1971 031Labeling Revision  
6/21/1973 030Labeling Revision  
1/5/1966 028Labeling Revision  
8/12/1964 027Labeling Revision  
10/24/1963 026Package Change  
5/27/1963 025Labeling Revision  
10/30/1961 022Labeling Revision  
4/7/1961 021Labeling Revision  
3/13/1961 020Control Supplement  
3/17/1960 019Labeling Revision  
7/31/1959 018Control Supplement  
2/6/1959 017Control Supplement  
1/14/1960 016Package Change  
8/18/1958 015Labeling Revision  
8/18/1958 014Labeling Revision  
7/18/1955 013Control Supplement  
11/20/1991 010Labeling Revision  
11/20/1991 008Labeling Revision  
11/20/1991 007Labeling Revision  
4/19/1957 006Labeling Revision  
3/4/1955 005Control Supplement  
11/29/1954 003Control Supplement  
9/24/1954 002Labeling Revision  
7/1/1954 000Approval  
 
There are no Therapeutic Equivalents
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