NDC 71335-3153 – Bupropion hydrochloride

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

Human Prescription Drug

Product NDC71335-3153

Product details

Brand name
Bupropion hydrochloride
Generic name
Bupropion hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211020
Marketed since
August 1, 2022
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
71335-3153-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3153-1)Jul 10, 2026
71335-3153-260 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3153-2)Jul 10, 2026
71335-3153-390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3153-3)Jul 10, 2026
71335-3153-4120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3153-4)Jul 10, 2026
71335-3153-514 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3153-5)Jul 10, 2026

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