NDC 71335-0182 – Bupropion Hydrochloride

Bupropion Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0182

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076143
Marketed since
January 17, 2006
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
71335-0182-160 TABLET, FILM COATED in 1 BOTTLE (71335-0182-1)Jul 24, 2018
71335-0182-230 TABLET, FILM COATED in 1 BOTTLE (71335-0182-2)Jun 20, 2018
71335-0182-3100 TABLET, FILM COATED in 1 BOTTLE (71335-0182-3)Jul 9, 2024
71335-0182-490 TABLET, FILM COATED in 1 BOTTLE (71335-0182-4)Mar 28, 2018
71335-0182-5120 TABLET, FILM COATED in 1 BOTTLE (71335-0182-5)Jul 9, 2024
71335-0182-615 TABLET, FILM COATED in 1 BOTTLE (71335-0182-6)Jul 9, 2024
71335-0182-721 TABLET, FILM COATED in 1 BOTTLE (71335-0182-7)Apr 28, 2021

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