NDC 50090-7602 – Bupropion Hydrochloride XL

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

Human Prescription Drug

Product NDC50090-7602

Product details

Brand name
Bupropion Hydrochloride XL
Generic name
Bupropion Hydrochloride
Labeler
A-S Medication Solutions
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090693
Marketed since
June 14, 2017
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
50090-7602-090 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7602-0)Jul 14, 2025

Other Bupropion hydrochloride products