Visitor Monitoring Drug History: PULMOLITE
 
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: PULMOLITE
FDA Application No: (NDA) 017776
Active Ingredient(s): TECHNETIUM TC-99M ALBUMIN AGGREGATED KIT
Company: CIS
 
Label History
 
Labels are not available on this site for PULMOLITE, (NDA) 017776
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/30/2002 019Manufacturing Change or Addition  
5/24/2001 018Manufacturing Change or Addition  
6/15/2000 016Manufacturing Change or Addition  
2/7/2000 015Manufacturing Change or Addition  
7/13/1999 014Control Supplement Letter 
3/24/1998 013Manufacturing Change or Addition  
10/1/1997 012Control Supplement  
1/25/1995 011Control Supplement  
5/2/1989 010Manufacturing Change or Addition  
5/19/1989 009Labeling Revision  
5/3/1985 008Control Supplement  
7/31/1992 007Control Supplement  
5/31/1983 006Control Supplement  
10/22/1985 005Practioner Draft Labeling  
7/24/1980 004Formulation Revision  
11/16/1976 000Approval  
 
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