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) 075311
Active Ingredient(s): FAMOTIDINE
Company: TEVA
 
Label History
 
View the label approved on June 4, 2004 for FAMOTIDINE, (ANDA) 075311


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/16/2001 000Approval Letter
Label
Review 
10/15/1998 000Tentative Approval Letter
Label
Review 
1/31/2001 000Tentative Approval Letter
Label
Review 
 
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