NDC 72189-124 – Bupropion Hydrochloride

Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC72189-124

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
DIRECT RX
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210497
Marketed since
August 14, 2020
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
72189-124-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-124-30)Aug 14, 2020
72189-124-72120 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-124-72)Aug 14, 2020

Other Bupropion hydrochloride products