Visitor Monitoring Drug Details: HEXADROL
 
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Drug Details

Drug Name: HEXADROL
FDA Application No: (NDA) 014694
Active Ingredient(s): DEXAMETHASONE SODIUM PHOSPHATE
Company: ORGANON USA INC
Original Approval or Tentative Approval Date: December 4, 1964
Chemical Type: 2 New active ingredient
Review Classification: S Standard review drug
 
 
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
HEXADROL DEXAMETHASONE SODIUM PHOSPHATEEQ 4MG PHOSPHATE/MLINJECTABLE; INJECTION Discontinued No None
HEXADROL DEXAMETHASONE SODIUM PHOSPHATEEQ 10MG PHOSPHATE/MLINJECTABLE; INJECTION Discontinued No None
HEXADROL DEXAMETHASONE SODIUM PHOSPHATEEQ 20MG PHOSPHATE/MLINJECTABLE; INJECTION Discontinued No None


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