NDC 71335-0135 – Bupropion Hydrochloride SR

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

Human Prescription Drug

Product NDC71335-0135

Product details

Brand name
Bupropion Hydrochloride SR
Generic name
Bupropion hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA079095
Marketed since
July 2, 2009
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
71335-0135-160 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-1)Sep 11, 2019
71335-0135-290 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-2)Sep 18, 2019
71335-0135-330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-3)Sep 11, 2019
71335-0135-4120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-4)Oct 8, 2024
71335-0135-545 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-5)Oct 8, 2024
71335-0135-6180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-6)Oct 8, 2024
71335-0135-728 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-7)Oct 8, 2024
71335-0135-856 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-8)Oct 8, 2024
71335-0135-9100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-9)Oct 8, 2024

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