Visitor Monitoring Drug Details: NICODERM CQ
 
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Drug Details

Drug Name: NICODERM CQ
FDA Application No: (NDA) 020165
Active Ingredient(s): NICOTINE
Company: SANOFI AVENTIS US
Original Approval or Tentative Approval Date: November 7, 1991
Chemical Type: 3 New dosage form
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
NICODERM CQ NICOTINE21MG/24HRFILM, EXTENDED RELEASE; TRANSDERMAL OTC Yes None
NICODERM CQ NICOTINE14MG/24HRFILM, EXTENDED RELEASE; TRANSDERMAL OTC Yes None
NICODERM CQ NICOTINE7MG/24HRFILM, EXTENDED RELEASE; TRANSDERMAL OTC Yes None


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