Visitor Monitoring Drug Details: CHOLESTYRAMINE
 
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Drug Details

Drug Name: CHOLESTYRAMINE
FDA Application No: (ANDA) 074554
Active Ingredient(s): CHOLESTYRAMINE
Company: TEVA PHARMS
Original Approval or Tentative Approval Date: October 2, 1996
 
 
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
CHOLESTYRAMINE CHOLESTYRAMINEEQ 4GM RESIN/PACKETPOWDER; ORAL Discontinued No None
CHOLESTYRAMINE CHOLESTYRAMINEEQ 4GM RESIN/SCOOPFULPOWDER; ORAL Discontinued No None


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