NDC 0615-8602 – Bupropion hydrochloride

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

Human Prescription Drug

Product NDC0615-8602

Product details

Brand name
Bupropion hydrochloride
Generic name
Bupropion hydrochloride
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA216800
Marketed since
May 31, 2023
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0615-8602-3930 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8602-39)Nov 4, 2025

Other Bupropion hydrochloride products