NDC 50090-4049 – Bupropion Hydrochloride XL

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

Human Prescription Drug

Product NDC50090-4049

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 · ANDA077715
Marketed since
November 26, 2008
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
50090-4049-090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4049-0)Jan 11, 2019
50090-4049-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4049-1)Jan 11, 2019
50090-4049-260 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4049-2)Jan 11, 2019

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