DEA Schedule CII
Strength
35 mg/1
Manufacturer
Teva Pharmaceuticals USA Inc.NDC
00093504601
Classification
Generic
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
DEXMETHYLPHENIDATE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA202731On Market Since
7/5/2017
Pharmacological Classes
Central Nervous System Stimulant
Central Nervous System Stimulation
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