DEA Schedule CII
Strength
36 mg/1
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
57664060888
Classification
Generic
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Last Updated
12/17/2025
Active Ingredients
METHYLPHENIDATE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA205135On Market Since
8/20/2020
Pharmacological Classes
Central Nervous System Stimulant
Central Nervous System Stimulation
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