NDC 82868-019 – Bupropion Hydrochloride SR

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

Human Prescription Drug

Product NDC82868-019

Product details

Brand name
Bupropion Hydrochloride SR
Generic name
Bupropion hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA205794
Marketed since
October 19, 2023
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
82868-019-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-019-30)Mar 14, 2024
82868-019-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-019-60)Oct 19, 2023
82868-019-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-019-90)Jan 2, 2025
82868-019-96180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-019-96)Feb 19, 2024

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