NDC 82804-013 – Bupropion Hydrochloride (XL)

Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC82804-013

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 · ANDA206556
Marketed since
August 29, 2016
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
82804-013-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-013-30)Sep 21, 2023
82804-013-6060 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-013-60)Sep 21, 2023
82804-013-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-013-90)Sep 21, 2023

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