NDC 23155-191 – bupropion Hydrochloride

Bupropion Hydrochloride 75 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC23155-191

Product details

Brand name
bupropion Hydrochloride
Generic name
bupropion Hydrochloride
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
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 (2)

Package NDCDescriptionSince
23155-191-01100 TABLET in 1 BOTTLE (23155-191-01)Aug 19, 2016
23155-191-101000 TABLET in 1 BOTTLE (23155-191-10)Aug 19, 2016

Recalls mentioning this NDC

Other Bupropion hydrochloride products