Bupropion Hydrobromide 68682-0581-30

Package NDC

68682-0581-30

Manufacturer: Oceanside Pharmaceuticals
Dosage Form: Tablet, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 29, 2026
Listing Expires: December 31, 2027
Application: NDA022108

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Active Ingredients

Ingredient	Strength
Bupropion Hydrobromide	348 mg/1

Drug Class

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

Selected Package

68682-0581-30Selected

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-581-30)