NDC 71335-0791 – bupropion Hydrochloride

Bupropion Hydrochloride 75 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0791

Product details

Brand name
bupropion Hydrochloride
Generic name
bupropion Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206975
Marketed since
August 19, 2016
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
71335-0791-130 TABLET in 1 BOTTLE (71335-0791-1)Apr 26, 2018
71335-0791-260 TABLET in 1 BOTTLE (71335-0791-2)Jun 19, 2019
71335-0791-390 TABLET in 1 BOTTLE (71335-0791-3)Jun 19, 2019
71335-0791-47 TABLET in 1 BOTTLE (71335-0791-4)Jun 19, 2019
71335-0791-514 TABLET in 1 BOTTLE (71335-0791-5)Jun 19, 2019
71335-0791-6120 TABLET in 1 BOTTLE (71335-0791-6)Jun 19, 2019
71335-0791-7100 TABLET in 1 BOTTLE (71335-0791-7)Jun 19, 2019

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