NDC 47335-737 – Bupropion hydrochloride

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

Human Prescription Drug 9 recalls

Product NDC47335-737

Product details

Brand name
Bupropion hydrochloride
Generic name
Bupropion hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078866
Marketed since
March 1, 2020
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
47335-737-08100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-08)Mar 1, 2020
47335-737-13500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-13)Mar 1, 2020
47335-737-8660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-86)Mar 1, 2020
47335-737-88100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-88)Mar 1, 2020

Recalls mentioning this NDC

Other Bupropion hydrochloride products