NDCFind

Bupropion 71335-0801-04

Generic: Bupropion Hydrochloride

Package NDC

71335-0801-04

Product NDC: 71335-0801

Manufacturer
Bryant Ranch Prepack
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
November 1, 2014
Listing Expires
December 31, 2026
Application
ANDA202304
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Active Ingredients

IngredientStrength
Bupropion Hydrochloride200 mg/1

Drug Class

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

Selected Package

71335-0801-04Selected

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-4)

Other packages for this product(5)

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-1)

180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-2)

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-3)

120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-5)

28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-6)