NDC 50090-6961 – Bupropion Hydrochloride XL

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

Human Prescription Drug

Product NDC50090-6961

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 · ANDA210015
Marketed since
April 30, 2023
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

Uses, dosage, side effects and warnings for Bupropion hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
50090-6961-030 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6961-0)Dec 19, 2023
50090-6961-190 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6961-1)Dec 19, 2023

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