NDC 33342-527 – Bupropion Hydrochloride (SR)

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

Human Prescription Drug

Product NDC33342-527

Product details

Brand name
Bupropion Hydrochloride (SR)
Generic name
Bupropion Hydrochloride
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA218567
Marketed since
June 23, 2026
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
33342-527-1090 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-527-10)Jun 23, 2026
33342-527-11100 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-527-11)Jun 23, 2026
33342-527-15500 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-527-15)Jun 23, 2026

Other Bupropion hydrochloride products