NDC 71335-1702 – Bupropion Hydrochloride SR

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

Human Prescription Drug

Product NDC71335-1702

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 · ANDA205794
Marketed since
April 20, 2018
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (9)

Package NDCDescriptionSince
71335-1702-160 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-1)Sep 16, 2020
71335-1702-290 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-2)Nov 20, 2020
71335-1702-330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-3)Oct 6, 2020
71335-1702-4120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-4)Apr 4, 2024
71335-1702-545 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-5)Apr 4, 2024
71335-1702-6180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-6)Sep 8, 2020
71335-1702-728 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-7)Apr 4, 2024
71335-1702-856 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-8)Apr 4, 2024
71335-1702-9100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-9)Apr 4, 2024

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