Visitor Monitoring Drug Details: GEODON
 
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Drug Details

Drug Name: GEODON
FDA Application No: (NDA) 020825
Active Ingredient(s): ZIPRASIDONE HYDROCHLORIDE
Company: PFIZER
Original Approval or Tentative Approval Date: February 5, 2001
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
GEODON ZIPRASIDONE HYDROCHLORIDEEQ 20MG BASECAPSULE; ORAL Prescription Yes None
GEODON ZIPRASIDONE HYDROCHLORIDEEQ 40MG BASECAPSULE; ORAL Prescription No None
GEODON ZIPRASIDONE HYDROCHLORIDEEQ 60MG BASECAPSULE; ORAL Prescription No None
GEODON ZIPRASIDONE HYDROCHLORIDEEQ 80MG BASECAPSULE; ORAL Prescription No None


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