NDCFind

Bupropion Hydrochloride 82804-0296

Product NDC

82804-0296
Manufacturer
Proficient Rx Lp
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
December 15, 2022
Listing Expires
December 31, 2027
Application
ANDA215568
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Active Ingredients

IngredientStrength
Bupropion Hydrochloride150 mg/1

Drug Class

Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]

Packaging Options(1)

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-296-90)