NDCFind

Bupropion Hydrochloride 67046-1572

Product NDC

67046-1572
Manufacturer
Coupler Llc
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
July 2, 2025
Listing Expires
December 31, 2026
Application
ANDA216800
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Active Ingredients

IngredientStrength
Bupropion Hydrochloride100 mg/1

Drug Class

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

Packaging Options(1)

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1572-3)