NDC 51655-098 – Bupropion Hydrochloride XL

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

Human Prescription Drug

Product NDC51655-098

Product details

Brand name
Bupropion Hydrochloride XL
Generic name
Bupropion Hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090693
Marketed since
September 6, 2022
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
51655-098-2690 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-098-26)Sep 6, 2022
51655-098-5230 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-098-52)Apr 7, 2023
51655-098-83180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-098-83)Jan 3, 2023

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