NDCFind

Bupropion Hydrochloride 50090-6353

Product NDC

50090-6353
Manufacturer
A-S Medication Solutions
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
December 15, 2021
Listing Expires
December 31, 2026
Application
ANDA075932
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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(4)

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6353-0)

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6353-1)

180 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6353-2)

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6353-3)