DEA Schedule CII
Strength
36 mg/1
Manufacturer
Actavis Pharma, Inc.NDC
62037072601
Classification
Generic
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
METHYLPHENIDATE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA076772On Market Since
3/4/2019
Pharmacological Classes
Central Nervous System Stimulant
Central Nervous System Stimulation
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