Visitor Monitoring Drug Details: KETALAR
 
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Drug Details

Drug Name: KETALAR
FDA Application No: (NDA) 016812
Active Ingredient(s): KETAMINE HYDROCHLORIDE
Company: PARKEDALE
Original Approval or Tentative Approval Date: February 19, 1970
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
KETALAR KETAMINE HYDROCHLORIDEEQ 10MG BASE/MLINJECTABLE; INJECTION Prescription Yes None
KETALAR KETAMINE HYDROCHLORIDEEQ 50MG BASE/MLINJECTABLE; INJECTION Prescription Yes AP
KETALAR KETAMINE HYDROCHLORIDEEQ 100MG BASE/MLINJECTABLE; INJECTION Prescription Yes AP


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