NDCFind

Bupropion Hydrochloride (xl) 50228-0144

Generic: Bupropion Hydrochloride

Product NDC

50228-0144
Manufacturer
Sciegen Pharmaceuticals,inc.
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
April 12, 2017
Listing Expires
December 31, 2027
Application
ANDA207479
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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(3)

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-144-05)

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-144-30)

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-144-90)