NDC 72789-377 – Bupropion Hydrochloride XL

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

Human Prescription Drug

Product NDC72789-377

Product details

Brand name
Bupropion Hydrochloride XL
Generic name
Bupropion hydrochloride
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210015
Marketed since
April 30, 2023
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
72789-377-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-377-90)Jan 30, 2024

Other Bupropion hydrochloride products