Visitor Monitoring Drug Details: ACTONEL
 
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Drug Details

Drug Name: ACTONEL
FDA Application No: (NDA) 020835
Active Ingredient(s): RISEDRONATE SODIUM
Company: PROCTER AND GAMBLE
Original Approval or Tentative Approval Date: March 27, 1998
Chemical Type: 1 New molecular entity (NME)
 
Therapeutic Equivalents Label Information
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
ACTONEL RISEDRONATE SODIUM30MGTABLET; ORAL Prescription No AB
ACTONEL RISEDRONATE SODIUM5MGTABLET; ORAL Prescription No AB
ACTONEL RISEDRONATE SODIUM35MGTABLET; ORAL Prescription Yes AB
ACTONEL RISEDRONATE SODIUM75MGTABLET; ORAL Prescription Yes None


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