Visitor Monitoring Drug History: IBUPROHM
 
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: IBUPROHM
FDA Application No: (ANDA) 070469
Active Ingredient(s): IBUPROFEN
Company: OHM LABS
 
Label History
 
Labels are not available on this site for IBUPROHM, (ANDA) 070469
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/5/1994 013Chemistry  
9/21/1992 012Chemistry  
8/22/1991 011Labeling in Effect  
8/23/1989 010Labeling  
4/7/1989 009Chemistry  
12/7/1988 008Chemistry  
7/22/1988 007Chemistry  
3/15/1989 006Labeling  
2/12/1988 005Chemistry  
2/12/1988 004Chemistry  
12/21/1987 003Chemistry  
6/27/1989 002Chemistry  
12/21/1987 001Chemistry  
8/29/1985 000Approval  
 
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