Visitor Monitoring Drug Details: OMEPRAZOLE
 
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Drug Details

Drug Name: OMEPRAZOLE
FDA Application No: (ANDA) 075347
Active Ingredient(s): OMEPRAZOLE
Company: ANDRX PHARMS
Original Approval or Tentative Approval Date: November 16, 2001
 
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
OMEPRAZOLE OMEPRAZOLE10MGCAPSULE, DELAYED REL PELLETS; ORAL Tentative Approval No None
OMEPRAZOLE OMEPRAZOLE20MGCAPSULE, DELAYED REL PELLETS; ORAL Tentative Approval No None
OMEPRAZOLE OMEPRAZOLE40MGCAPSULE, DELAYED REL PELLETS; ORAL Tentative Approval No None


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