Visitor Monitoring Drug Details: HABITROL
 
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Drug Details

Drug Name: HABITROL
FDA Application No: (NDA) 020076
Active Ingredient(s): NICOTINE
Company: NOVARTIS
Original Approval or Tentative Approval Date: November 27, 1991
Chemical Type: 3 New dosage form
Review Classification: S Standard 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
HABITROL NICOTINE7MG/24HRFilm, Extended Release; Transdermal Discontinued No None
HABITROL NICOTINE14MG/24HRFilm, Extended Release; Transdermal Discontinued No None
HABITROL NICOTINE21MG/24HRFilm, Extended Release; Transdermal Discontinued No None
HABITROL NICOTINE7MG/24HRFILM, EXTENDED RELEASE; TRANSDERMAL OTC Yes None
HABITROL NICOTINE14MG/24HRFILM, EXTENDED RELEASE; TRANSDERMAL OTC Yes None
HABITROL NICOTINE21MG/24HRFILM, EXTENDED RELEASE; TRANSDERMAL OTC Yes None


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