Visitor Monitoring Drug History: CIMETIDINE
 
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: CIMETIDINE
FDA Application No: (ANDA) 075122
Active Ingredient(s): CIMETIDINE
Company: LEK PHARMS
 
Label History
 
Labels are not available on this site for CIMETIDINE, (ANDA) 075122
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/20/2002 005Manufacturing Revision  
5/2/2000 002Control Supplement  
11/27/2000 001Labeling  
6/19/1998 000Approval Letter 
5/28/1998 000Tentative Approval Letter 
 
Therapeutic Equivalents
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