Visitor Monitoring Drug Details: RENAGEL
 
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Drug Details

Drug Name: RENAGEL
FDA Application No: (NDA) 021179
Active Ingredient(s): SEVELAMER HYDROCHLORIDE
Company: GENZYME
Original Approval or Tentative Approval Date: July 12, 2000
Chemical Type: 3 New dosage form
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
RENAGEL SEVELAMER HYDROCHLORIDE400MGTABLET; ORAL Prescription No None
RENAGEL SEVELAMER HYDROCHLORIDE800MGTABLET; ORAL Prescription Yes None


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