NDC 67046-1572 – Bupropion hydrochloride

Bupropion Hydrochloride 100 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC67046-1572

Product details

Brand name
Bupropion hydrochloride
Generic name
Bupropion hydrochloride
Labeler
Coupler LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA216800
Marketed since
July 2, 2025
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
67046-1572-330 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1572-3)Jul 2, 2025

Other Bupropion hydrochloride products