NDC 71335-1986 – Bupropion Hydrochloride SR

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

Human Prescription Drug

Product NDC71335-1986

Product details

Brand name
Bupropion Hydrochloride SR
Generic name
bupropion hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211347
Marketed since
November 2, 2020
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
71335-1986-160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-1)Nov 4, 2021
71335-1986-290 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-2)Jul 18, 2024
71335-1986-330 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-3)Jul 18, 2024
71335-1986-445 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-4)Jul 18, 2024
71335-1986-528 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-5)Jul 18, 2024
71335-1986-6120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-6)Dec 29, 2022

Other bupropion hydrochloride products