Visitor Monitoring Drug Details: ACTOS
 
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Drug Details

Drug Name: ACTOS
FDA Application No: (NDA) 021073
Active Ingredient(s): PIOGLITAZONE HYDROCHLORIDE
Company: TAKEDA GLOBAL
Original Approval or Tentative Approval Date: July 15, 1999
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority 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
ACTOS PIOGLITAZONE HYDROCHLORIDEEQ 15MG BASETABLET; ORAL Prescription No None
ACTOS PIOGLITAZONE HYDROCHLORIDEEQ 30MG BASETABLET; ORAL Prescription No None
ACTOS PIOGLITAZONE HYDROCHLORIDEEQ 45MG BASETABLET; ORAL Prescription Yes None


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