NDCFind

Bupropion Hydrochloride 85534-0006-09

Package NDC

85534-0006-09

Product NDC: 85534-0006

Manufacturer
Hawaii Repack, Inc.
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
February 17, 2015
Listing Expires
December 31, 2026
Application
ANDA077285
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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

85534-0006-09Selected

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-9)

Other packages for this product(4)

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-1)

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-3)

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-5)

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-6)