NDC 71205-291 – Bupropion Hydrochloride XL

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

Human Prescription Drug

Product NDC71205-291

Product details

Brand name
Bupropion Hydrochloride XL
Generic name
Bupropion Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA207224
Marketed since
October 1, 2017
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
71205-291-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-291-30)Jul 1, 2019
71205-291-6060 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-291-60)Jul 1, 2019
71205-291-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-291-90)Jul 1, 2019

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