Visitor Monitoring Drug Details: LOTENSIN
 
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Drug Details

Drug Name: LOTENSIN
FDA Application No: (NDA) 019851
Active Ingredient(s): BENAZEPRIL HYDROCHLORIDE
Company: NOVARTIS
Original Approval or Tentative Approval Date: June 25, 1991
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
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
LOTENSIN BENAZEPRIL HYDROCHLORIDE5MGTABLET; ORAL Prescription No AB
LOTENSIN BENAZEPRIL HYDROCHLORIDE10MGTABLET; ORAL Prescription No AB
LOTENSIN BENAZEPRIL HYDROCHLORIDE20MGTABLET; ORAL Prescription No AB
LOTENSIN BENAZEPRIL HYDROCHLORIDE40MGTABLET; ORAL Prescription Yes AB


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