NDC 72162-1526 – Bupropion Hydrochloride (XL)

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

Human Prescription Drug

Product NDC72162-1526

Product details

Brand name
Bupropion Hydrochloride (XL)
Generic name
Bupropion hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA207479
Marketed since
April 12, 2017
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
72162-1526-330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72162-1526-3)Apr 12, 2017
72162-1526-5500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72162-1526-5)Apr 12, 2017

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