High Outlier
DEA Schedule CII
Strength
10 mg/1
Manufacturer
Azurity Pharmaceuticals Inc.NDC
24338002603
Classification
Brand (ANDA)
Dosage Form
TABLET
Route
ORAL
Last Updated
6/18/2025
Active Ingredients
AMPHETAMINE SULFATEApproval Type
Generic (ANDA)
FDA Application
ANDA200166On Market Since
11/1/2015
Pharmacological Classes
Central Nervous System Stimulant
Central Nervous System Stimulation
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