Visitor Monitoring Drug Details: DAYTRANA
 
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Drug Details

Drug Name: DAYTRANA
FDA Application No: (NDA) 021514
Active Ingredient(s): METHYLPHENIDATE
Company: SHIRE
Original Approval or Tentative Approval Date: April 6, 2006
Chemical Type: 23 New active ingredient and new dosage form
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
DAYTRANA METHYLPHENIDATE10MG/9HR (1.1MG/HR)FILM, EXTENDED RELEASE; TRANSDERMAL Prescription Yes None
DAYTRANA METHYLPHENIDATE15MG/9HR (1.6MG/HR)FILM, EXTENDED RELEASE; TRANSDERMAL Prescription Yes None
DAYTRANA METHYLPHENIDATE20MG/9HR (2.2MG/HR)FILM, EXTENDED RELEASE; TRANSDERMAL Prescription Yes None
DAYTRANA METHYLPHENIDATE30MG/9HR (3.3MG/HR)FILM, EXTENDED RELEASE; TRANSDERMAL Prescription Yes None


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