Visitor Monitoring Drug Details: TENSILON
 
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Drug Details

Drug Name: TENSILON
FDA Application No: (NDA) 007959
Active Ingredient(s): EDROPHONIUM CHLORIDE
Company: VALEANT PHARM INTL
Original Approval or Tentative Approval Date: May 3, 1951
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
 
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
TENSILON EDROPHONIUM CHLORIDE10MG/MLINJECTABLE; INJECTION Prescription Yes AP
TENSILON PRESERVATIVE FREE EDROPHONIUM CHLORIDE10MG/MLINJECTABLE; INJECTION Prescription Yes AP


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