Strength
150 mg/1
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
47335073788
Classification
Generic
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Last Updated
2/18/2026
Active Ingredients
BUPROPION HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA078866On Market Since
3/1/2020
Pharmacological Classes
Aminoketone
Dopamine Uptake Inhibitors
Increased Dopamine Activity
Increased Norepinephrine Activity
Norepinephrine Uptake Inhibitors
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