Visitor Monitoring Drug Details: ACIPHEX
 
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Drug Details

Drug Name: ACIPHEX
FDA Application No: (NDA) 020973
Active Ingredient(s): RABEPRAZOLE SODIUM
Company: EISAI MEDCL RES
Original Approval or Tentative Approval Date: August 19, 1999
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
 
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
ACIPHEX RABEPRAZOLE SODIUM10MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**TABLET, DELAYED RELEASE; ORAL Discontinued No None
ACIPHEX RABEPRAZOLE SODIUM20MGTABLET, DELAYED RELEASE; ORAL Prescription Yes AB


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