NDC 71205-967 – Bupropion Hydrochloride (XL)

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

Human Prescription Drug

Product NDC71205-967

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 · ANDA210081
Marketed since
August 30, 2018
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
71205-967-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-967-30)Jun 9, 2020
71205-967-55500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-967-55)Jun 9, 2020
71205-967-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-967-90)Jun 9, 2020

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