NDC 50090-7334 – Bupropion Hydrochloride (XL)

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

Human Prescription Drug

Product NDC50090-7334

Product details

Brand name
Bupropion Hydrochloride (XL)
Generic name
Bupropion hydrochloride
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA207479
Marketed since
April 12, 2017
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
50090-7334-030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7334-0)Oct 15, 2024
50090-7334-190 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7334-1)Oct 15, 2024

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