Visitor Monitoring Drug Details: REGROTON
 
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Drug Details

Drug Name: REGROTON
FDA Application No: (NDA) 015103
Active Ingredient(s): CHLORTHALIDONE; RESERPINE
Company: SANOFI AVENTIS US
Original Approval or Tentative Approval Date: May 8, 1964
Chemical Type: 4 New combination
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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
DEMI-REGROTON CHLORTHALIDONE; RESERPINE25MG; 0.125MGTABLET; ORAL Discontinued No None
REGROTON CHLORTHALIDONE; RESERPINE50MG; 0.25MGTABLET; ORAL Discontinued No None


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