NDC 82804-080 – Bupropion Hydrochloride XL

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

Human Prescription Drug

Product NDC82804-080

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 · ANDA210015
Marketed since
April 30, 2023
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
82804-080-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-080-30)Mar 5, 2024
82804-080-6060 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-080-60)Mar 5, 2024
82804-080-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-080-90)Mar 5, 2024

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