68968-5553 : Daytrana 15 mg/9h Transdermal Patch


NDC: 68968-5553
Labeler: Noven Therapeutics, LLC
Product Type: Human Prescription Drug
Drug Name:  Daytrana
Dosage Form: Transdermal Patch
Application #: NDA021514
Rev. Date: 
CSA Schedule: CII (US) [1]


[1] Schedule II / IIN Controlled Substance: High potential for abuse which may lead to severe psychological or physical dependence. (i.e. Narcotics such as Dilaudid, Methadone, Demerol, Oxycodone, Percocet, Fentanyl, Morphine, Opium, Codeine, and Hydrocodone ... Schedule IIN stimulants include non-narcotic Amphetamines such as Dexedrine, Adderall, Desoxyn, Methylphenidate (Ritalin) ... Other Schedule II substances include Amobarbital, Glutethimide, and Pentobarbital. More Details: US Dept of Justice Controlled Substance Schedules.

NDC Package Codes:

  • 68968-5553-3: 30 PATCH IN 1 CARTON (68968‑5553‑3) > 9 H IN 1 PATCH

Active Ingredients:

  • Methylphenidate

Dosage Strength:

  • 15 mg/9h

Pharmaceutical Classes:

  • Central Nervous System Stimulant [EPC]
  • Central Nervous System Stimulation [PE]

Related Products:

Based on records with the same trade name.
  • 68968-5552 Daytrana 10 mg/9h Transdermal Patch by Noven Therapeutics, LLC
  • 68968-5554 Daytrana 20 mg/9h Transdermal Patch by Noven Therapeutics, LLC
  • 68968-5555 Daytrana 30 mg/9h Transdermal Patch by Noven Therapeutics, LLC

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.