Visitor Monitoring Drug Details: FAMOTIDINE
 
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Drug Details

Drug Name: FAMOTIDINE
FDA Application No: (ANDA) 077352
Active Ingredient(s): FAMOTIDINE
Company: PERRIGO
Original Approval or Tentative Approval Date: July 27, 2005
 
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
FAMOTIDINE FAMOTIDINE40MGTABLET; ORAL Prescription No AB
FAMOTIDINE FAMOTIDINE20MGTABLET; ORAL Prescription No AB


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