NDC 62135-723 – Bupropion Hydrochloride

Bupropion Hydrochloride 75 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC62135-723

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Chartwell RX, LLC
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
62135-723-9090 TABLET in 1 BOTTLE (62135-723-90)Aug 11, 2023

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