Visitor Monitoring Drug Details: NORTRIPTYLINE HYDROCHLORIDE
 
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Drug Details

Drug Name: NORTRIPTYLINE HYDROCHLORIDE
FDA Application No: (ANDA) 073667
Active Ingredient(s): NORTRIPTYLINE HYDROCHLORIDE
Company: TEVA
Original Approval or Tentative Approval Date: April 11, 1996
 
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
NORTRIPTYLINE HYDROCHLORIDE NORTRIPTYLINE HYDROCHLORIDEEQ 10MG BASECAPSULE; ORAL Discontinued No None
NORTRIPTYLINE HYDROCHLORIDE NORTRIPTYLINE HYDROCHLORIDEEQ 25MG BASECAPSULE; ORAL Discontinued No None
NORTRIPTYLINE HYDROCHLORIDE NORTRIPTYLINE HYDROCHLORIDEEQ 50MG BASECAPSULE; ORAL Discontinued No None
NORTRIPTYLINE HYDROCHLORIDE NORTRIPTYLINE HYDROCHLORIDEEQ 75MG BASECAPSULE; ORAL Discontinued No None


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