Visitor Monitoring Drug History: FAMOTIDINE
 
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: FAMOTIDINE
FDA Application No: (ANDA) 075650
Active Ingredient(s): FAMOTIDINE
Company: ACTAVIS ELIZABETH
 
Label History
 
Labels are not available on this site for FAMOTIDINE, (ANDA) 075650
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/7/2002 002Control Supplement  
4/23/2002 001Control Supplement  
9/14/2001 000Approval Letter
Letter
Review 
3/17/2000 000Tentative Approval Letter
Letter
Review 
 
Therapeutic Equivalents
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