NDC 51655-115 – Bupropion Hydrochloride SR

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

Human Prescription Drug

Product NDC51655-115

Product details

Brand name
Bupropion Hydrochloride SR
Generic name
Bupropion hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211347
Marketed since
October 5, 2022
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
51655-115-2560 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-25)Oct 5, 2022
51655-115-2690 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-26)Nov 15, 2022
51655-115-5230 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-52)Nov 30, 2022
51655-115-83180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-83)Jan 5, 2023

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