NDC 71335-2649 – Bupropion hydrochloride

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

Human Prescription Drug

Product NDC71335-2649

Product details

Brand name
Bupropion hydrochloride
Generic name
Bupropion hydrochloride
Labeler
Bryant Ranch Prepack
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 (7)

Package NDCDescriptionSince
71335-2649-160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-1)Jun 3, 2025
71335-2649-230 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-2)Jun 3, 2025
71335-2649-3100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-3)Jun 3, 2025
71335-2649-490 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-4)Jun 3, 2025
71335-2649-5120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-5)Jun 3, 2025
71335-2649-615 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-6)Jun 3, 2025
71335-2649-721 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-7)Jun 3, 2025

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