NDC 42806-348 – Bupropion Hydrochloride XL

Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC42806-348

Product details

Brand name
Bupropion Hydrochloride XL
Generic name
Bupropion Hydrochloride
Labeler
Epic Pharma, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA207224
Marketed since
October 1, 2017
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

Uses, dosage, side effects and warnings for Bupropion hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
42806-348-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-348-05)May 29, 2018
42806-348-0990 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-348-09)Oct 1, 2017
42806-348-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-348-30)Oct 1, 2017

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