Visitor Monitoring Drug Details: BENZEDRINE
 
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Drug Details

Drug Name: BENZEDRINE
FDA Application No: (ANDA) 083900
Active Ingredient(s): AMPHETAMINE SULFATE
Company: SMITH KLINE & FRENCH
Original Approval or Tentative Approval Date: February 26, 1976
 
 
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
BENZEDRINE AMPHETAMINE SULFATE5MGTablet; Oral Discontinued No None
BENZEDRINE AMPHETAMINE SULFATE10MGTablet; Oral Discontinued No None


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