Visitor Monitoring Drug Details: ZIPRASIDONE HYDROCHLORIDE
 
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Drug Details

Drug Name: ZIPRASIDONE HYDROCHLORIDE
FDA Application No: (ANDA) 077560
Active Ingredient(s): ZIPRASIDONE HYDROCHLORIDE
Company: LUPIN PHARMS
Original Approval or Tentative Approval Date: May 16, 2007
 
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
ZIPRASIDONE HYDROCHLORIDE ZIPRASIDONE HYDROCHLORIDE20MGCAPSULE; ORAL Tentative Approval No None
ZIPRASIDONE HYDROCHLORIDE ZIPRASIDONE HYDROCHLORIDE40MGCAPSULE; ORAL Tentative Approval No None
ZIPRASIDONE HYDROCHLORIDE ZIPRASIDONE HYDROCHLORIDE60MGCAPSULE; ORAL Tentative Approval No None
ZIPRASIDONE HYDROCHLORIDE ZIPRASIDONE HYDROCHLORIDE80MGCAPSULE; ORAL Tentative Approval No None


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