Visitor Monitoring Drug Details: JANIMINE
 
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Drug Details

Drug Name: JANIMINE
FDA Application No: (NDA) 017895
Active Ingredient(s): IMIPRAMINE HYDROCHLORIDE
Company: ABBOTT
Original Approval or Tentative Approval Date: November 15, 1974
Chemical Type: 6 New indication
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
JANIMINE IMIPRAMINE HYDROCHLORIDE10MGTABLET; ORAL Discontinued No None
JANIMINE IMIPRAMINE HYDROCHLORIDE25MGTABLET; ORAL Discontinued No None
JANIMINE IMIPRAMINE HYDROCHLORIDE50MGTABLET; ORAL Discontinued No None


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