NDCFind

Bupropion Hydrochloride Xl 00591-3331-30

Generic: Bupropion Hydrochloride

Package NDC

00591-3331-30

Product NDC: 00591-3331

Manufacturer
Actavis Pharma, Inc.
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
November 26, 2008
Listing Expires
December 31, 2027
Application
ANDA077715
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Active Ingredients

IngredientStrength
Bupropion Hydrochloride150 mg/1

Drug Class

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

Selected Package

00591-3331-30Selected

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3331-30)

Other packages for this product(2)

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3331-05)

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3331-19)