NDC 50090-7349 – Bupropion hydrochloride

Bupropion Hydrochloride 100 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC50090-7349

Product details

Brand name
Bupropion hydrochloride
Generic name
Bupropion hydrochloride
Labeler
A-S Medication Solutions
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA216800
Marketed since
May 31, 2023
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
50090-7349-060 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7349-0)Oct 16, 2024

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