Visitor Monitoring Drug History: UROCIT-K
 
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: UROCIT-K
FDA Application No: (NDA) 019071
Active Ingredient(s): POTASSIUM CITRATE
Company: MISSION PHARMA
 
Label History
 
Labels are not available on this site for UROCITK, (NDA) 019071
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/13/2002 008Manufacturing Change or Addition  
12/26/2000 006Control Supplement  
3/1/1999 005Manufacturing Change or Addition  
8/31/1992 004Formulation Revision  
10/30/1992 003Labeling Revision  
8/31/1992 002Control Supplement  
1/13/1986 001Labeling Revision  
8/30/1985 000Approval  
 
Therapeutic Equivalents
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