NDCFind

Bupropion Hydrochloride 59651-0846-01

Package NDC

59651-0846-01

Product NDC: 59651-0846

Manufacturer
Aurobindo Pharma Limited
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
June 3, 2025
Listing Expires
December 31, 2026
Application
ANDA090325
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Active Ingredients

IngredientStrength
Bupropion Hydrochloride100 mg/1

Drug Class

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

Selected Package

59651-0846-01Selected

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-846-01)

Other packages for this product(1)

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-846-05)