Visitor Monitoring Drug History: DIAMOX
 
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: DIAMOX
FDA Application No: (NDA) 008943
Active Ingredient(s): ACETAZOLAMIDE
Company: DURAMED PHARMS BARR
 
Label History
 
Labels are not available on this site for DIAMOX, (NDA) 008943
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/5/1999 048Package Change  
2/14/1991 047Control Supplement  
11/28/1990 046Labeling Revision  
4/23/1990 045Control Supplement  
1/24/1990 044Labeling Revision  
12/6/1989 043Labeling Revision  
7/21/1988 042Expiration Date Change  
6/22/1988 041Labeling Revision  
8/11/1987 040Labeling Revision  
6/16/1987 039Control Supplement  
10/6/1987 038Control Supplement  
3/3/1987 037Labeling Revision  
3/21/1986 036Labeling Revision  
5/13/1985 035Labeling Revision  
9/25/1984 034Control Supplement  
2/22/1984 033Formulation Revision  
9/29/1982 032Control Supplement  
4/2/1982 031Package Change  
6/12/1981 030Formulation Revision  
12/17/1980 029Formulation Revision  
12/17/1980 028Formulation Revision  
12/17/1980 027Control Supplement  
8/30/1979 026Formulation Revision  
2/14/1984 025Control Supplement  
7/31/1979 024Control Supplement  
10/2/1978 023Labeling Revision  
4/7/1978 022Control Supplement  
4/3/1978 021Formulation Revision  
1/9/1978 020Control Supplement  
6/29/1977 019Control Supplement  
6/29/1977 018Formulation Revision  
6/6/1977 017Expiration Date Change  
1/28/1977 015Expiration Date Change  
1/28/1977 013Formulation Revision  
7/27/1953 000Approval  
 
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