Visitor Monitoring Drug History: K+10
 
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: K+10
FDA Application No: (ANDA) 070999
Active Ingredient(s): POTASSIUM CHLORIDE
Company: ALRA
 
Label History
 
Labels are not available on this site for K10, (ANDA) 070999
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/23/1995 007Chemistry  
6/23/1995 006Chemistry  
7/22/1994 005Chemistry  
11/16/1992 004SBA  
10/22/1987 000Approval  
 
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