Visitor Monitoring Drug History: NEBUPENT
 
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: NEBUPENT
FDA Application No: (NDA) 019887
Active Ingredient(s): PENTAMIDINE ISETHIONATE
Company: ABRAXIS PHARM
 
Label History
 
Labels are not available on this site for NEBUPENT, (NDA) 019887
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/19/1996 007Labeling Revision  
3/29/1996 006Labeling Revision  
5/31/1994 005Control Supplement  
3/22/1996 004Control Supplement  
3/5/1996 002New or Modified Indication  
8/21/1989 001Manufacturing Change or Addition  
6/15/1989 000Approval  
 
There are no Therapeutic Equivalents
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