Visitor Monitoring Drug Details: ZYPREXA ZYDIS
 
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Drug Details

Drug Name: ZYPREXA ZYDIS
FDA Application No: (NDA) 021086
Active Ingredient(s): OLANZAPINE
Company: LILLY
Original Approval or Tentative Approval Date: April 6, 2000
Chemical Type: 3 New dosage form
Review Classification: S Standard 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
ZYPREXA ZYDIS OLANZAPINE5MGTABLET, ORALLY DISINTEGRATING; ORAL Prescription Yes None
ZYPREXA ZYDIS OLANZAPINE10MGTABLET, ORALLY DISINTEGRATING; ORAL Prescription No None
ZYPREXA ZYDIS OLANZAPINE15MGTABLET, ORALLY DISINTEGRATING; ORAL Prescription No None
ZYPREXA ZYDIS OLANZAPINE20MGTABLET, ORALLY DISINTEGRATING; ORAL Prescription No None


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