NDC 50090-7110 – Bupropion Hydrochloride (XL)

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

Human Prescription Drug

Product NDC50090-7110

Product details

Brand name
Bupropion Hydrochloride (XL)
Generic name
Bupropion hydrochloride
Labeler
A-S Medication Solutions
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
50090-7110-090 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7110-0)Mar 11, 2024
50090-7110-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7110-1)Mar 11, 2024
50090-7110-260 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7110-2)Mar 11, 2024

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