Visitor Monitoring Drug History: IBUPROFEN
 
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: IBUPROFEN
FDA Application No: (ANDA) 076112
Active Ingredient(s): IBUPROFEN
Company: DR REDDYS LABS INC
 
Label History
 
Labels are not available on this site for IBUPROFEN, (ANDA) 076112
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/31/2001 000Approval Review 
 
Therapeutic Equivalents
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