Visitor Monitoring Drug Details: AVENTYL HYDROCHLORIDE
 
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Drug Details

Drug Name: AVENTYL HYDROCHLORIDE
FDA Application No: (NDA) 014684
Active Ingredient(s): NORTRIPTYLINE HYDROCHLORIDE
Company: LILLY
Original Approval or Tentative Approval Date: November 6, 1964
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard 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
AVENTYL HYDROCHLORIDE NORTRIPTYLINE HYDROCHLORIDEEQ 10MG BASECAPSULE; ORAL Discontinued No None
AVENTYL HYDROCHLORIDE NORTRIPTYLINE HYDROCHLORIDEEQ 25MG BASECAPSULE; ORAL Discontinued No None


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