Visitor Monitoring Drug History: PARADIONE
 
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: PARADIONE
FDA Application No: (NDA) 006800
Active Ingredient(s): PARAMETHADIONE
Company: ABBOTT
 
Label History
 
Labels are not available on this site for PARADIONE, (NDA) 006800
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/24/1989 015Manufacturing Change or Addition  
12/2/1987 014Manufacturing Change or Addition  
12/7/1984 013Expiration Date Change  
6/28/1982 012Control Supplement  
7/14/1980 010Labeling Revision  
10/24/1979 008Control Supplement  
7/29/1975 005Control Supplement  
6/15/1949 000Approval  
 
There are no Therapeutic Equivalents
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