Visitor Monitoring Drug Details: HALFAN
 
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Drug Details

Drug Name: HALFAN
FDA Application No: (NDA) 020250
Active Ingredient(s): HALOFANTRINE HYDROCHLORIDE
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: July 24, 1992
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
O Orphan 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
HALFAN HALOFANTRINE HYDROCHLORIDE250MGTABLET; ORAL Discontinued No None


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