Visitor Monitoring Drug Details: RENORMAX
 
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Drug Details

Drug Name: RENORMAX
FDA Application No: (NDA) 020240
Active Ingredient(s): SPIRAPRIL HYDROCHLORIDE
Company: SCHERING
Original Approval or Tentative Approval Date: December 29, 1994
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
O Orphan drug
 
There are no 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
RENORMAX SPIRAPRIL HYDROCHLORIDE3MGTABLET; ORAL Discontinued No None
RENORMAX SPIRAPRIL HYDROCHLORIDE6MGTABLET; ORAL Discontinued No None
RENORMAX SPIRAPRIL HYDROCHLORIDE12MGTABLET; ORAL Discontinued No None
RENORMAX SPIRAPRIL HYDROCHLORIDE24MGTABLET; ORAL Discontinued No None


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