NDC 71335-1837 – Bupropion Hydrochloride SR

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

Human Prescription Drug

Product NDC71335-1837

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 (9)

Package NDCDescriptionSince
71335-1837-160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-1)May 5, 2021
71335-1837-290 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-2)Feb 17, 2022
71335-1837-330 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-3)Apr 26, 2021
71335-1837-4120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-4)Jul 17, 2024
71335-1837-545 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-5)Jul 17, 2024
71335-1837-6180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-6)Feb 2, 2022
71335-1837-728 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-7)Jul 17, 2024
71335-1837-856 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-8)Jul 17, 2024
71335-1837-9100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-9)Jul 17, 2024

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