NDC 71335-0877 – bupropion Hydrochloride

Bupropion Hydrochloride 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0877

Product details

Brand name
bupropion Hydrochloride
Generic name
bupropion Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207389
Marketed since
May 26, 2018
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
71335-0877-160 TABLET in 1 BOTTLE (71335-0877-1)Sep 7, 2018
71335-0877-230 TABLET in 1 BOTTLE (71335-0877-2)Jun 21, 2018
71335-0877-3100 TABLET in 1 BOTTLE (71335-0877-3)Dec 27, 2021
71335-0877-490 TABLET in 1 BOTTLE (71335-0877-4)Sep 13, 2018
71335-0877-5120 TABLET in 1 BOTTLE (71335-0877-5)Dec 27, 2021
71335-0877-615 TABLET in 1 BOTTLE (71335-0877-6)Dec 27, 2021
71335-0877-721 TABLET in 1 BOTTLE (71335-0877-7)Dec 27, 2021

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