NDCFind

Bupropion Hydrochloride (xl) 80425-0539-02

Generic: Bupropion Hydrochloride

Package NDC

80425-0539-02

Product NDC: 80425-0539

Manufacturer
Advanced Rx Of Tennessee, Llc
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
August 29, 2025
Listing Expires
December 31, 2026
Application
ANDA207479
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Active Ingredients

IngredientStrength
Bupropion Hydrochloride300 mg/1

Drug Class

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

Selected Package

80425-0539-02Selected

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80425-0539-2)

Other packages for this product(2)

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80425-0539-1)

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80425-0539-3)