Visitor Monitoring Drug Details: REGITINE
 
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Drug Details

Drug Name: REGITINE
FDA Application No: (NDA) 008278
Active Ingredient(s): PHENTOLAMINE MESYLATE
Company: NOVARTIS
Original Approval or Tentative Approval Date: January 30, 1952
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
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
REGITINE PHENTOLAMINE MESYLATE5MG/VIALINJECTABLE; INJECTION Prescription Yes AP


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