NDC 72162-2400 – bupropion Hydrochloride

Bupropion Hydrochloride 75 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72162-2400

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 (1)

Package NDCDescriptionSince
72162-2400-1100 TABLET in 1 BOTTLE (72162-2400-1)Oct 2, 2024

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