Visitor Monitoring Drug Details: PRILOSEC
 
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Drug Details

Drug Name: PRILOSEC
FDA Application No: (NDA) 019810
Active Ingredient(s): OMEPRAZOLE
Company: ASTRAZENECA
Original Approval or Tentative Approval Date: September 14, 1989
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
PRILOSEC OMEPRAZOLE20MGCAPSULE, DELAYED REL PELLETS; ORAL Prescription Yes AB
PRILOSEC OMEPRAZOLE40MGCAPSULE, DELAYED REL PELLETS; ORAL Prescription Yes None
PRILOSEC OMEPRAZOLE10MGCAPSULE, DELAYED REL PELLETS; ORAL Prescription No AB


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