Visitor Monitoring Drug History: MICRO-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: MICRO-K
FDA Application No: (NDA) 018238
Active Ingredient(s): POTASSIUM CHLORIDE
Company: KV PHARM
 
Label History
 
Labels are not available on this site for MICROK, (NDA) 018238
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/20/2003 031Labeling Revision Letter 
5/8/2000 029Manufacturing Change or Addition  
7/10/2000 028Manufacturing Change or Addition  
3/9/2000 027Manufacturing Change or Addition  
1/13/1998 026Manufacturing Change or Addition  
8/19/1993 025Manufacturing Change or Addition  
3/12/1990 024Manufacturing Change or Addition  
1/30/1998 023Labeling Revision  
1/30/1998 022Labeling Revision  
6/30/1988 021Package Change  
12/10/1987 020Control Supplement  
6/26/1987 019Package Change  
10/23/1986 018Control Supplement  
2/14/1986 017Manufacturing Change or Addition  
11/25/1985 016Formulation Revision  
8/8/1985 014Control Supplement  
7/25/1985 013Package Change  
3/16/1984 012Formulation Revision  
5/14/1984 011General Efficacy (MarkIV)  
5/4/1983 010Control Supplement  
8/3/1983 009Control Supplement  
8/23/1982 007Other Amendment  
3/3/1982 006Formulation Revision  
3/3/1982 005Formulation Revision  
3/8/1982 004Package Change  
2/17/1982 003Package Change  
6/2/1981 002Control Supplement  
2/13/1981 001Manufacturing Change or Addition  
10/17/1980 000Approval  
 
Therapeutic Equivalents
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