NDC 50090-6871 – Bupropion Hydrochloride SR

Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC50090-6871

Product details

Brand name
Bupropion Hydrochloride SR
Generic name
bupropion hydrochloride
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA205794
Marketed since
April 20, 2018
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

Uses, dosage, side effects and warnings for bupropion hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
50090-6871-060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-0)Dec 4, 2023
50090-6871-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-1)Dec 4, 2023
50090-6871-2180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-2)Dec 4, 2023
50090-6871-390 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-3)Dec 4, 2023

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